Überblick über die Statistik des Gehaltsniveaus für "Project Coordinator in Deutschland"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, Pharmacology, Pharmacovigilance, Pharmacy, Phase I, pipetting, PMP, Policy, Post Marketing, Postdoctoral research, Post-marketing, Preclinical, Pricing & Reimbursement, Pricing and Reimbursement, PROC, Process Excellence, Procurement, Product Management, Project Leadership, Project Management, PromoMats, Protein Characterisation, protocol development, Protocol writing, PSURs, Public Affairs, publishing, Purchasing, QP, Qualification Visit, Quality Assurance, Quality Control, Quality Management, Quality Management System, Radiology, Randomisation, Randomization, Rave, Reactovigilance, Real World Evidence, Recruitment, Regional Monitoring, Regulatory, Regulatory Operations, Regulatory submissions, Regulatory Systems Management, remote monitoring, RFI, Risk Management, risk-based monitoring, RMA, RMP, SAE, SAE reporting, Sales Inventory, Sample size estimation, Samples, SAS, Scrum, SDS-PAGE, SDTM, Serialisation, Shipments, shipping, Simoa, Site contracts, Site Engagement, site payments, SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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Location: Poland- Home based        Schedule: Freelance, Various FTEs                                    CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Poland. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.      Who will you be working for?      About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      Our Company Ethos   Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.      Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: PolandShare: LinkedIn Facebook Twitter Email

Location: Germany- Home based        Schedule: Freelance, Various FTEs                                  CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Germany. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                      As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.      Who will you be working for?      About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      Our Company Ethos   Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.      Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: GermanyShare: LinkedIn Facebook Twitter Email

Location: Spain - Home based          Schedule: Freelance, Various FTEs                                      CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Clinical Project Manager II, to join their clinical operations team in Spain. This is a full-time opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                          As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                                    Join our team and help us deliver clinical trials that will improve patients' lives.            Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project-specific trainingOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager, and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process     Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.            If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.          Who will you be working for?          About CROMSOURCE        CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                          Our Company Ethos     Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.          CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.          Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation  Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, ICH-GCP, Project Management, EnglishLocation: SpainShare: LinkedIn Facebook Twitter Email

Location: Germany- Home based        Schedule: Freelance, Various FTEs                                     CROMSOURCE is a growing international CRO dedicated to a quality-focused approach with a collaborative "one-team" culture, and we are looking for a dynamic person to join our in-house team as a Freelance Senior Clinical Project Manager,  You will be working on projects from our varied client base, ranging from small to mid-sized pharma, biotech, and medical device companies.       As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines, and other applicable regulations.                         Join our team and help us deliver clinical trials that will improve patients' lives.        Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projectsManage all project-specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team membersKeep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assignedKnowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areasAssure the proper timelines of the assigned projectsManage the budget for the projectMonitor the workload and the performance of the project teamPlan and monitor the tasks of the team in the specific areasCoordinate the Clinical Research Associates and Clinical Monitors activityCollaborate with the Clinical Trial Administrators and Clinical Research Associates in terms of local authorities' approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activitiesAssist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDelivering  project specific trainingsOrganise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetingsProvide project updates to the Sponsor, Senior Project Manager,  and Project Director/Leader as requiredInform the Project Director/Leader about any issuesPerform co-monitoring visits for the assigned clinical projects as necessaryAct as a tutor for Project Coordinators and Project Managers IMaintain relationships with the Sponsor, including providing project updatesPrepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying with and enforcing Company procedures Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similarExcellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Application Process   Once you have submitted your CV, you will receive an acknowledgment email. If you have the requirements we need, you will be invited for a phone interview as the first step.        If you would like to discuss the role before applying through the website @ www.cromsource.com/careers/job-vacancies please contact [email protected] for more information.      Who will you be working for?      About CROMSOURCE      CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.                      Our Company Ethos   Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. Continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates.      CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status, or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.      Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research Organisation                         Skills: Clinical Project Manager, Clinical Study Manager, clinical trials, Project Management, Study ManagementLocation: GermanyShare: LinkedIn Facebook Twitter Email

Curious about the future of event marketing?SpotMe is the enterprise event platform to manage engaging events that help accelerate customer relationships at scale. Trusted by 12,000+ global Fortune 500 business leaders and loved by 10,000,000+ users, brands like J&J, Deloitte, and Red Hat use SpotMe to manage hybrid, virtual, and in-person events with a branded, personalized and compliant experience and get deep data insights that flow into their CRM.Behind the magic stands a curious, diligent, and humble team with over 30 nationalities. A team that feels great pride in the work they do, a team that cares for each other, and a team that is always ready for the next challenge.Mission:Support in delivering Onsite, Virtual, and Hybrid eventsResponsibilities:Onsite supportRequired frequent travel to destinations worldwide.Provide assistance to participants.Set up and deliver live interactivity.Set up and rehearse onsite with the client and AV team before the event.Facilitate engagement activities.Act as the primary point of contact with the client onsite.Update content to the app whilst onsite.Virtual support Schedule and deliver speaker briefing sessions.Participate/Lead the project kick-off and reviews with the project lead and clients.Run speaker green rooms during live sessions.Use our powerful Backstage CMS to tailor-make the clients’ apps and to ensure the best participants' experience before, during, and after the event.Be the main point of contact for the client during live sessions, handling platform updates and user escalations.Live monitoring of the platform and reporting on the metrics of the event.Fully manage and deliver small-scale projects.This role can potentially lead up to a Project Manager position (still contractor based).Requirements:At least two years experience in event management (stage management, speaker coordination, other relevant).Demonstrable experience of onsite event management or coordination.Have a modern computer, equipped with Google Chrome and MS Office.If using a Mac, Apple M1 Processor and 16 GB RAMIf using a PC, Intel i7 processor and 16 GB RAM.Have a stable Internet connection (wifi / wired), with a bandwidth of at least 20Mbps down, 10Mbps up.A mobile with 4G / 5G to fallback on if needed.Eligible to travel internationally.Clean basic background check.At least 18 years old.Based in Germany.Accessible to a major international airport.Fluent in English. Fluent also in German.Registered as a sole trader, self-employed, or owner and employee of your company, in Germany.More information:You can find more information here:Technical assessment and supporting resources detailsOur Talent Network FAQSpotMe recruits, compensates, and promotes regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, parental status, or veteran status.

Location: Netherlands - Home based  Schedule: Permanent, Full-time                       Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their internal team in Netherlands. This role is a full-time permanent opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                 As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                         Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Benefits of Working in Netherlands:Competitive SalaryGroup health insuranceGreat pension scheme24 vacation daysInternet reimbursementCompany Car with fuel card depending on the function.Dedicated Line Manager The Application Process         Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step. If you would like to discuss the role before applying through the website @

Location: Belgium - Home based    Schedule: Permanent, Full-time                           Do you want to join a team that is passionate about making a difference in drug and medical device development?  CROMSOURCE, a growing CRO, is recruiting for a Senior Clinical Project Manager to join their internal team in Belgium. This role is a full-time permanent opportunity. You will work on projects from our varied client base, ranging from small to mid-sized pharma and medical device companies.                                  As a Senior Clinical Project Manager, you will be responsible for managing the clinical projects ensuring quality of the services in accordance with contractual obligations, applicable SOPs, ICH-GCP guidelines and other applicable regulations.                             Main Tasks and Responsibilities:Manage and coordinate the assigned clinical projects.Manage all project specific services required by the Sponsor (central lab exams, drug shipments, document shipments, etc.)Manage the correct development of the clinical project, interacting with the Sponsor and the Investigators and properly coordinating the project team members.Keep professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assigned.Knowledgeable in the application process for clinical studies, in force in the country/ies of work.Collect and manage study data documentation (CRFs, patient diaries, questionnaires, queries, study supplies, regulatory documents, correspondence, etc.)May act as a Technical Specialist supervising the projects within specific therapeutic and technical areas.Assure the proper timelines of the assigned projects.Manage the budget for the project.Monitor the workload and the performance of the project team.Plan and monitor the tasks of the team in the specific areas.Coordinate the Clinical Research Associates and Clinical Monitors activity.Collaborate with he Clinical Trial Administrators and Clinical Research Associates in terms of local authorities approval activitiesCollaborate in the overall management of the project with the assigned Biometrics team and with all other project team members involved in the delivery of specific activities (such as Safety, Regulatory, etc.)Collaborate with the CTAs in archiving activities.Assist the Medical Monitor in preparing protocols, Case Report Forms, and final Clinical Study ReportsDeliver project specific trainings.Organise and participate in Monitor and Investigator MeetingsOrganise or take part in the periodic project update meetings.Provide project updates to the Sponsor, Senior Project Manager and Project Director/Leader as required.Inform the Project Director/Leader about any issues.Perform co-monitoring visits for the assigned clinical projects as necessary.Act as a tutor for Project Coordinators and Project Manager IMaintain relationships with the Sponsor, including providing project updates.Prepare the SOPs relating to clinical research activities in collaboration with the Quality System UnitCollaborate in complying and enforcing Company procedures. Education and Experience Required:University Degree in scientific, medical, or paramedical disciplinesProven experience in clinical project management activities, 5 plus years in the CRO/pharmaceutical industry including previous experience as a CRA or similar.Excellent knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirementsFluent in English and local language(s)Proficiency in Microsoft Office (e.g., Word, Excel, Outlook)Willingness to travel The Benefits of Working in Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursement The Application Process           Once you have submitted your CV, you will receive an acknowledgement email. If you have the requirements we need, you will be invited for phone interview as the first step.                        If you would like to discuss the role before applying through the website @ http://www.cromsource.com/careers/job-vacancies please send an mail to: [email protected] for more information.                     Who will you be working for?                                            About CROMSOURCE                           CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus on the heart of everything we do.                                                            Our Company Ethos                      Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.                                                         CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.                                             Keywords: Senior Project Manager, Clinical Project Manager, Senior Study Manager, Study Management Associate, Project Management Associate, Clinical, Drugs, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Clinical Study Management, Project Leader, Project Lead, CRO, Clinical Research Organisation, Contract Research OrganisationSkills: Clinical Project Manager, Clinical Study Manager, Clinical Trial Manager, Senior Clinical Project Manager, clinical trials, CRO, Medical Devices, Study ManagementLocation: BelgiumShare: LinkedIn Facebook Twitter Email

Start your mission at Bentley now! Become an important part of our international team and work together with us to give people around the world a better quality of life. Support us on our way to a successful future with innovative products for minimally invasive treatment of vascular diseases. We promise a diverse work environment with good career opportunities with an exceptional employer!We offer an internship within the international sales department for approx. 6 months at Bentley InnoMed in Hechingen.We look forward to receiving your application documents in English.Your missionYou support our international sales team and the management in ongoing processes and projectsThrough your interface function you create process optimisations and communicate in English and German between stakeholdersYou carry out analyses and research independentlyYou take over the sub-project management for a specific project Your profileYou are studying economics, preferably specialising in sales, strategic business, general management, business analytics or a comparable field of study Ideally you have already gained practical experience in sales or in dynamic corporate structuresYour language skills in English and German are at least at C1 level and you have knowledge of project managementYou are passionate, enthusiastic and enjoy sales and are characterised by a structured, analytical, independent and solution-oriented way of workingYou have a very good command of MS Office and can quickly familiarise yourself with new IT tools thanks to your affinity for toolsWhy us?It is our agile and appreciative corporate culture with flat hierarchies and quick decision-making that distinguishes our dynamic and efficient work. All areas of responsibility act independently, characterized by our startup mentality combined with the structure and power of an established company. Flexible working hours, regular team events, training and development opportunities allow you to advance your development according to your individual needs. Are you ready for Bentley? #yourmissionstartsnowIf you have any questions, please contact Sarah Hofmann at 07471 984995 645. Online application Standort Bentley InnoMed GmbH, Hechingen

Job Summary :Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the DACH region, specifically in Munich, Germany. Clinical Trial Managers with expertise in CNS and Neuroscience are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility after probation to the DACH region only with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.Responsibilities :Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulationsServe as primary Sponsor contact for operational project-specific issues and study deliverablesMaintain in depth knowledge of protocol, therapeutic area, and indicationProvide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is providedReview and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicableDevelop operational project plansManage risk assessment and executionResponsible for management of study vendorManage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverablesQualifications :Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;Experience in Phases 1-4; Phases 2-3 preferred;Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred;5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;Management of overall project timeline;Bid defense experience preferred; andStrong leadership skills.Medpace Overview :Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace? :People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace PerksHybrid work-from-home options (dependent upon position and level)Competitive PTO packagesCompany-sponsored employee appreciation events Employee health and wellness initiativesFlexible work scheduleCompetitive compensation and benefits packageStructured career paths with opportunities for professional growthAwardsRecognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. EO/AA Employer M/F/Disability/Vets Über das Unternehmen:Medpace, Inc.

All about us finding simple solutions.As the Brand Relations & Retail Media team we develop the ideal strategy for each of our partners. The Brand Relations team manages our partner brands marketing campaigns and strategic development within the ABOUT YOU marketing ecosystem. The Product Manager team manages the campaign go live to performance evaluations, optimizes processes and manages the implementation of new native advertising concepts. The Event Cooperations team then conceptualizes the individual integration at our ABOUT YOU events. All three departments share the same goal: monetizing the ABOUT YOU platform through long-term strategic cooperations.You will be responsible for the reporting of our partners’ campaigns in the fashion sector. We are looking for a motivated Working Student (m/f/d) in the area of Analytics and Development in our Brand Relations & Retail Media Department.ResponsibilitiesEvaluation of our 360° campaigns and creation of presentations for various national and international fashion and non-fashion brandsAnalysis of the performance of onsite, newsletter and organic & paid social media placementsQuality assurance of brand campaigns after Go-Live in cooperation with the Product Managers & Account ManagersDerivation of recommendations for action to optimize subsequent campaignsProject responsibilities e.g. in the course of process optimizations or data analysisSupport in the preparation of analyses for strategy meetings with various fashion brandsRequirementsStudies in the field of business administration, statistics, marketing or similarFirst work experience in the context of an internship or a student trainee in online marketing/analytical field is an advantageGood knowledge of Microsoft Office, especially ExcelAt least basic knowledge in dealing with online marketing KPIsIdeally initial knowledge of Google AnalyticsStrong analytical thinking skills and enjoy working with numbersIndependent and structured way of workingVery good knowledge of EnglishYou are a passionate team playerBenefitsHybrid working Fresh fruit every day Sports courses Exclusive employee discounts Free drinks Language courses Company parties Mobility subsidy Central Location Flexible Working Hours Dog-friendly office AY Academy Feedback Culture Our team consists of experts from a wide range of fields: Whether fashion, marketing, business or tech – we are united by our passion for what we do. We motivate and support each other, share our know-how and are open to other opinions and new ideas.We look forward to receiving your application – preferably online via our application portal. This way we can guarantee a faster process and it is also very easy for you to upload your application documents! :-)

Deine AufgabenDu bist verantwortlich für die Projektplanung und Task-ErstellungDu übernimmst die tägliche Anpassung & Pflege unseres PlanungstoolsDu bist zuständig für unsere Zeit- und Ressourcenplanung inkl. QualitätsmanagementDu bist der Sparringspartner für unsere Account Manager, Design und Content DirektorenDu kümmerst dich um unsere internen ProjekteDein ProfilDu hast ein abgeschlossenes Studium oder eine erfolgreich abgeschlossene Ausbildung Du hast bereits Agenturerfahrung im digitalen UmfeldDu hast erste Erfahrung in der Betreuung von KundenprojektenDu kennst Dich aus im digitalen MarketingDu beherrschst gängige Planungstechniken und ToolsOrganisieren liegt Dir im Blut Du hast deine Stärken und Spaß an strukturiertem, selbständigem und eigenverantwortlichem ArbeitenStrukturiertes, selbstständiges und eigenverantwortliches Arbeiten zählt zu Deinen Stärken und bereitet Dir FreudeDu denkst konzeptionell und hast ein technisches GrundverständnisDu hast ein gesteigertes Qualitätsbewusstsein und bist den Entwicklungen im digitalen Marketing gegenüber aufgeschlossenMit Deinem Auftreten kannst Du andere begeistern und bist kommunikationsstarkDu hast sehr gute Deutschkenntnisse in Wort und Schrift und Deine Englischkenntnisse enden nicht bei "Hello“ und "Goodbye“Wir trauen Dir Großes zu! Bei uns kannst Du vieles lernen. Daher freuen wir uns auch dann über Deine Bewerbung, wenn Du nicht alle Punkte erfüllst.Das kannst Du von uns erwartenEin dynamisches und spannendes Agenturumfeld mit wirklich tollen Kollegen und einer fairen Work-Life-Balance. Denn wir wollen, dass Du lange bei uns bleibst!Kontinuierliche Aus- und Weiterbildung im sich am schnellsten entwickelnden Umfeld der digitalen MedienlandschaftFlache Hierarchien und schnelle Übernahme von VerantwortungHervorragende AufstiegsmöglichkeitenModerne und hochwertige ArbeitsausstattungWir bieten Dir flexible ArbeitszeitenDu hast die Wahl! Home-Office oder OfficeBenefitsDynamisch, aktiv und immer einen Schritt voraus: Damit es allen unseren fleißigen und motivierten Köpfen rundum gut geht, sorgen wir für abwechslungsreiche Aktionen und attraktive Annehmlichkeiten.Urban Sports Mitgliedschaft mit ArbeitgeberzuschussNextbike Mitgliedschaft mit 60 Freiminuten pro AusleiheCorporate Benefits Mitarbeiterrabatte für diverse Online ShopsNimm Dir Zeit für Dich: 2 Mental Health Days pro Jahr & regelmäßig mobile Massage im OfficeUnbegrenzter Zugang zu Trainings auf LinkedIn Learning Familienservice von voiio: Plattform mit Angeboten wie virtueller Kinderbetreuung, Yoga Sessions und vielfältigen BeratungsangebotenMitarbeiter-Café mit leckerem Kaffee, Getränken, einer Müsli-Bar und frischem ObstTolle Parties, Agentur-Events und Kicker-Turniere Über unsAls unabhängige Marketing-Agentur steht add2 für digitale Kommunikation. Von A bis Z. Seit 1997 lotsen wir unsere Kunden durch digitale Gewässer wie Content- und Social-Media-Marketing, Dynamic Video und Audio oder Display- und Programmatic-Advertising. Was immer unsere Kunden bewegt, gemeinsam sorgen wir für die passende Lösung. Hand in Hand und immer mit dem Blick aufs Ganze. Unsere bunt gemischte HafenCrew besteht aus Menschen mit den unterschiedlichsten Talenten. Du kannst also auf jede Menge Know-how aus vielen Köpfen zurückgreifen. So lernen wir täglich voneinander und arbeiten dabei eng zusammen. Wie du siehst, wird der Teamgedanke bei uns großgeschrieben. Den möchten wir durch gemeinsame Aktivitäten wie Agentur-Events, Team-Essen und Feierabendbiere in gemütlicher Runde fördern. Und das Beste: Wir arbeiten da, wo andere Urlaub machen. Mit direktem Blick auf den Medienhafen können wir auch mal abschalten und kreative Gedanken tanken. Und wenn das nicht ausreicht, bietet dir unser gemütliches Mitarbeitercafé mit Kicker, kostenlosem Obstkorb und Getränken das perfekte Ambiente, um sich mit deinen Team-Kollegen und Kolleginnen auszutauschen. Solltest du einmal im Home-Office sein, dann kannst du dich einfach über Teams mit deiner Hafen-Crew austauschen. Standort add2 GmbH, Düsseldorf

Lyric Automation Germany GmbH, with its locations in Hamburg, Langenhagen near Hanover, and Munich, specializes in sales, project management and after-sales service for high-quality automation systems and acts as a link between the parent company Guangdong Lyric Robot Automation and the European market. Lyric Robot is a high-tech company with over 10,000 employees and is a manufacturer of high-end automation systems in the areas of automotive and consumer batteries, automotive parts, precision electronics and rail transport. The company has a dominant position in the Chinese market and also exports its intelligent manufacturing solutions to Europe, the USA, Canada, Mexico, Japan, India and the Middle East.AufgabenBills and Contracts management.Financial records and reports preparationFinancial software management, for example, DATEV, SAPResponsible for sorting out VAT issues and communicating with tax accountants on various financial issues.Responsible for preparing project technical service contracts and pre-sales service contracts.Budget and cost management.Bank and financing communication, handling related consultations such as guarantee financing.Assisting our HQ to transfer funds to overseas and other subsidiaries and affiliated companies legally and compliantly.Audit work cooperation.QualifikationFinancial expertise: In-depth understanding of German accounting and tax regulations as well as basic knowledge of international financial standards. Analytical and problem-solving skills: Ability to analyze financial data, identify potential problems and develop effective solutions.Communication skills: Fluent in English and German, knowledge of Chinese is an advantage. Clear, accurate and effective communication with internal team members, external partners (such as banks, tax advisors) and international colleagues (China, Poland) is required.Knowledge of financial software and office software: Basic knowledge of the financial software DATEV and skilled use of office software such as Excel to process complex tables and financial reports.Teamwork: Working with team members to complete projects and tasks together. Intercultural communication skills: The ability to communicate effectively and work in different cultural contexts is very important due to international coordination.If you enjoy designing or independently developing your area of responsibility, we would like to get to know you. Please send us your documents, your salary expectations, and your possible starting date.Your contact for your application:Jiefei Shi, HR departmentLyric Automation Germany GmbHDie Lyric Automation Germany GmbH mit ihren Standorten in Hamburg, Langenhagen bei Hannover, und München ist auf den Vertrieb, das Projektmanagement und den After-Sales-Service von hochwertigen Automatisierungsanlagen spezialisiert und fungiert als Verbindung der Muttergesellschaft Guangdong Lyric Robot Automation zum europäischen Markt. Lyric Robot ist ein High-Tech-Unternehmen mit über 7.000 Mitarbeitern und ist Hersteller von High-End-Automatisierungsanlagen in den Bereichen Automotive- und Consumer-Batterien, Automobilteile, Präzisionselektronik und Schienenverkehr. Das Unternehmen verfügt über eine dominante Position im chinesischen Markt, exportiert seine intelligenten Fertigungslösungen auch nach Europa, die USA, Kanada, Mexiko, Japan, Indien und in den Mittleren Osten. Standort Lyric Automation Germany GmbH, Langenhagen

ZEIT MEDIA.ZEIT MEDIA ist die Sales Organisation der ZEIT Verlagsgruppe. Unsere Mission: Gemeinsam stark kommunizieren. Uns interessiert, was unsere Kund:innen bewegen möchten. Gemeinsam entwickeln wir kraftvolle Kommunikationslösungen, um die richtigen Zielgruppen optimal über alle Medien-Kanäle der ZEIT zu erreichen.Verbinde Marken und Inhalte.DIE ZEIT Verlagsgruppe wächst kontinuierlich und stellt dazu ihre Vermarktung noch zukunftsorientierter auf. Nutze diese Chance und werde Teil dieses erfolgreichen Teams! Zur Unterstützung unseres Teams in Hamburg suchen wir zum nächstmöglichen Zeitpunkt und in unbefristeter Anstellung einen Concept Coordinator (d/w/m) in Vollzeit.Als Concept Coordinator berichtest du an den Head Brand & Concept Solutions im Bereich ZEIT MEDIA und übernimmst schwerpunktmäßig die folgenden Aufgaben:Du bist als Projektmanager und One-face-to-the-customer​ verantwortlich für die professionelle Umsetzung portfolioübergreifender Mediakonzepte.Du unterstützt das Concepter-Team bei der Erstellung kreativer, kundenindividueller Mediakonzepte nach Briefing der Media Sales Manager bzw. anhand von Kunden- oder Mediaagentur-Briefings.Du setzt die Projekte nach Abschluss professionell um. Von der Vertragserstellung über Kampagnenoptimierung bis zum Reporting und die Koordination und Steuerung aller beteiligten Gewerke liegt die Verantwortung bei dir.Du hast den Überblick über alle Produkte, Marken, Ad Specials und weitere Angebote innerhalb des ZEIT MEDIA-Portfolios.Du kannst die Kundenbedürfnisse gut einschätzen, so dass du durch die Projektbetreuung Potentiale für Upselling und Anschlussprojekte erkennst und dem Sales Manager mitteilst.Crossmedial und kommunikationsstark - Dein Profil.Du verfügst über ein abgeschlossenes kommunikationswissenschaftliches oder medienwissenschaftliches Studium oder eine adäquate praxisorientierte Ausbildung.Idealerweise hast du bereits mehrjährige Berufserfahrung im B2B-Marketing eines Medienunternehmens oder einer Kommunikationsagentur gesammelt und bringst daher Erfahrung in der Nutzung von Projektmanagementtools mit.Du hast Erfahrung in der Koordination und Steuerung von Projektteams und begreifst die Betreuung komplexer Themen und anspruchsvoller Kunden als Chance.Durch deinen crossmedialen Hintergrund siehst du die digitale Transformation des Medienmarktes als Chance. Du trittst selbstbewusst auf und zeichnest dich durch deine Kommunikationsstärke und deine Offenheit für Neues aus. Du überzeugst uns mit einer schnellen Auffassungsgabe, einer strukturierten und gründlichen Arbeitsweise.Klingt nach dir? Dann freuen wir uns über deine Bewerbung inkl. einem aussagekräftigen CV sowie Arbeitszeugnissen.Unser Engagement für deine Entwicklung.Dazulernen: Weiterbildung ist uns wichtig. Deshalb bieten wir allen Mitarbeitenden über unsere ZEIT AKADEMIE, die Produkte von ZEIT SPRACHEN, dem Holtzbrinck E-Learning Campus oder Blinkist vielfältige Möglichkeiten zur individuellen Entwicklung. Einmal im Jahr nutzen wir den internen ZEIT University Day sowie regelmäßige University Snacks, um uns zu verschiedenen Themen auszutauschen und voneinander zu lernen.Arbeitsort und - zeit nach individuellen Bedürfnissen: Unsere Arbeitsumgebung ist geprägt von Flexibilität und Individualität. Wir bieten flexible Arbeitszeiten wie Gleitzeit und mobiles Arbeiten sowie vielfältige Teilzeitmodelle, um die Balance zwischen Beruf und Privatleben optimal zu gestalten. Zusätzlich befinden sich unsere Arbeitsplätze in zentraler Lage mit exzellenter Anbindung an den öffentlichen Nahverkehr – einen Zuschuss zum Deutschlandticket und für ein JobRad gibt es natürlich auch.Vergünstigungen: Wir lieben unsere Produkte, daher steht dir die gesamte Bandbreite unserer Publikationen, Veranstaltungen und Medienangebote kostenfrei zur Verfügung. Zusätzlich bieten wir zu Mitarbeiterkonditionen verschiedene Zeitungs- und Zeitschriftenabonnements sowie unsere ZEIT Shop Produkte an. Über die Plattformen Corporate Benefits und benefit.me kannst du außerdem von vielen Vergünstigungen für Museen, Theater, Festivals, verschiedene Produkte oder Konferenzen profitieren. Individuelle Unterstützung: Das ganzheitliche Unterstützungsprogramm “Employee Assistance Program“ bietet Dir schnelle und wirkungsvolle Hilfe bei beruflichen und privaten Fragestellungen – auch in besonderen Krisensituationen.Kommunikation und Austausch werden bei uns großgeschrieben. Durch verschiedene interne Formate und Projekte, wie z.B. unserem Mentor:innen - und Pat:innen-Programm, einem monatlichen All Hands und begleitenden Newslettern oder beim Mystery Lunch fördern wir Vernetzung und Austausch. Erste Einblicke findest du bei kununu, LinkedIn ,  XING oder auch auf unserer  ZEIT Karriereseite. Solange diese Position auf unserer Karriereseite sichtbar ist, kannst du dich sehr gerne darauf bewerben - es gibt keine Bewerbungsfrist. Weitere Antworten zu unserem Bewerbungsprozess findest du in unseren FAQ. Wir kümmern uns umeinander.Die ZEIT Verlagsgruppe ist ein Arbeitgeber, der für Chancengleichheit und einen respektvollen Umgang steht. Wir setzen uns ein für faire Beschäftigungsmöglichkeiten unabhängig von ethnischer oder sozialer Herkunft, Geschlecht, Religion, Weltanschauung, Alter, sexueller Identität oder Behinderung. Unser stetiges Ziel ist es, ein wertschätzendes und anerkennendes Arbeitsumfeld für alle Beschäftigten zu schaffen. Über das Unternehmen:Zeitverlag Gerd Bucerius GmbH & Co. KG

Abiomed is an innovative medical device business with an inspiring mission "Patients First" and a unique guiding company principle "Recovering hearts. Saving lives." With more than 2,000 employees, Abiomed is one of the fastest growing medical technology businesses in the world with corporate headquarters in Danvers, USA, and locations in Aachen and Berlin, Germany, Tokyo, Japan, and Singapore. Abiomed is part of Johnson & Johnson MedTech.Abiomed is an employer with attractive working conditions and an appreciative corporate culture that focuses on the needs of its employees. Abiomed inspires and retains exceptional talent through collaboration, passion and continuous development.Clinical Trial CoordinatorThe Clinical Trial Coordinator (CTC) supports Clinical Project and Program Managers in planning and coordinating activities in all aspects of clinical trial operations. This position requires appropriate interpretation of significant policies and procedures. It involves interaction with internal and external customers and partners, and must operate with a high degree of discretion, as the role involves handling information of a confidential and critical nature.Main tasks and responsibilities:Plan, coordinate, and arrange study communications and meetings on and off-site with both internal and external attendeesPrepare all necessary documents for the evaluation of new proposals and coordinate the decision process of new AR or ISS projectsManage the grant application platform which maintains all necessary documents and the communication with PIsSet up, update, maintain and close Trial Master Files. Assure currency and accuracy of required clinical trials documents Maintain project-specific regulatory document inventory systems which include a precise quality check (QC) process when documents are receivedCommunicate with investigator sites on collection of regulatory documentsCreate study materials, including newsletters, study updates, etc. under the direction of a Scientist or Clinical Program ManagerSource and distribute study suppliesInteract with Finance departments to support invoice processingInteract with the Sales and Customer service department to support and coordinate external needs and internal processes.Under guidance of Clinical Operations management, interact with internal stakeholders and external clients to coordinate the accomplishment of business needsRequirements:BS degree or BS degreeRelevant clinical or basic research experience working at an Investigator Site, Sponsor or Clinical Research OrganizationFamiliarity of clinical trial operations, ICH, GCP Guidelines Good working experience in a team environment across multi-functional areasHighly organized, self-motivated, detail-oriented, proactive, and accurateAbility to work with urgency and thrive in a high-energy, fast-paced environmentDemonstrate excellent communication, verbal and written, and interpersonal skillsFluent in written and spoken English and GermanDemonstrate proficiency in MS Office Suite: Word, PowerPoint, Excel, Project ABIOMED is an Equal Employment Opportunity employer. We are committed to the policy of providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, disability or national origin. Über das Unternehmen:Johnson and Johnson

Company DescriptionAbout UbisoftUbisoft’s 21,000 team members, working across more than 30 countries around the world, are bound by a common mission to enrich players’ lives with original and memorable gaming experiences. Their commitment and talent have brought to life many acclaimed franchises such as Assassin’s Creed, Far Cry, Watch Dogs, Just Dance, Rainbow Six, and many more to come. Ubisoft is an equal opportunity employer that believes diverse backgrounds and perspectives are key to creating worlds where both players and teams can thrive and express themselves. If you are excited about solving game-changing challenges, cutting edge technologies and pushing the boundaries of entertainment, we invite you to join our journey and help us create the unknown.About Ubisoft MainzThe teams at Ubisoft Mainz are engineering some of Ubisoft’s biggest blockbusters. Operating from a historic city in the heart of Germany, the studio develops games pushing the limits of the genre like the acclaimed Anno 1800 and lends decades of expertise to AAA co-development projects like Tom Clancy’s Rainbow Six Siege and the upcoming Beyond Good And Evil 2. More information at mainz.ubisoft.com.Job DescriptionFor a yetunannounced project developed at Ubisoft Mainz we are looking for a Game Writer (f/m/d). This new project, not related to the ANNO series, has a strong narrative focus, so it is your opportunity to shine! You would work in such varied areas as dialogue writing, systemic game texts, world building, story, and character development. You will be part of a carefully selected and highly motivated team of developers. Your responsibilities: Write in-game-text and dialogue following form and contentCreate characters and the subsequent text and voice linesCreation and support of the audio bookSupport the conception of narrative conceptsSupport story and world building (lore)Work with internal tools to manage text creation, localization, and version controlLecture and rework 3rd party text contentsCreate additional game text for UI and marketingClosely collaborate with all disciplines inside a focused teamQualificationsWhat you bring:Valid experience as a game, screen, or creative writerExcellent writing skillsNative English language levelA broad area of interest exceeding gamesTeam player with a positive mindsetA superior motivation to create high quality contentBonus:Ability to work with digital text management toolsKnowledge and interest in psychology, philosophy, and historyInterest in literature (e.g. Poe, Lovecraft, Jackson, Maurier) and pop culture (horror)German language skills are a plusWhat to send our way: Your CV, highlighting your education, experience, and skillsA cover letter including your earliest starting date, expected salary and why you would like to join us Please provide samples of your writing/previous work with your application.Additional InformationWhat we offer:Relocation support: We offer financial support in form of a cash allowance and assistance with accommodation search and settle-in support via our relocation partner, for international candidates we offer visa assistance Ubisoft Blue Byte Academy: We offer multiple opportunities for you to discover your full potential and develop yourself in various areas. Guest speakers from the industry, workshops, and access to our training and development platform as well as to our in-house libraryDiscounted and free games: Discount on employee game orders & free Ubisoft games on Ubisoft Connect Hybrid work model: Provides the flexibility to combine working from the studio and your home within GermanyMonthly Mobility Budget: 80€ per month that can be used on bicycle lease, parking spot rental or public transportation ticket Up to 350€ childcare support per child per month Company Pension Scheme: We offer an attractive company pension scheme Gym subsidy: We contribute 50% (up to a maximum amount of 25€) towards the monthly cost of a gym membership of your choice English and German online lessons for free: Good to know: Our main language in the studio is English 26 days paid vacation per year Corporate Benefits web portal: Employee discount program for affiliated retailers, shops, and service providers We offer a highly motivating challenge for team players interested in showing personal initiative in an innovative and international company. If you are passionate about video games and would like to join an industry leader - please apply via our career portal. For further information, please check https://mainz.ubisoft.com/en/Über das Unternehmen:Ubisoft

Curious about the future of event marketing?SpotMe is the enterprise event platform to manage engaging events that help accelerate customer relationships at scale. Trusted by 12,000+ global Fortune 500 business leaders and loved by 10,000,000+ users, brands like J&J, Deloitte, and Red Hat use SpotMe to manage hybrid, virtual, and in-person events with a branded, personalized and compliant experience and get deep data insights that flow into their CRM.Behind the magic stands a curious, diligent, and humble team with over 30 nationalities. A team that feels great pride in the work they do, a team that cares for each other, and a team that is always ready for the next challenge.Mission: Responsible for delivering Virtual, Hybrid and In-person events from kickoff to post-meeting review.Responsible for coordinating internal resources and customer teams for Virtual and Hybrid events creation.Responsibilities:Lead projects following our high-quality standards and best practices to ensure great client experience. Make sure all of the events are executed within the agreed deadlines.Use our powerful Backstage CMS to tailor-make the clients’ apps and to ensure the best participants' experience before, during, and after the event.Be a Backstage subject-matter expert for our customers.Brief and manage the assigned operations team (Live coordinator,Live producer, Onsite coordinator)Requirements & Skills:Fluent in EnglishFluent in German and any another language will be considered a strong advantageExcellent organizational and prioritization skills, always meeting deadlines.Detail-oriented, high-standards achiever without excusesExcellent computer skills and tech-savvinessProficiency with Microsoft packages (PowerPoint, Excel, Word) or Google WorkspaceRequired to travel onsite for up to 3 events per month during busy seasons Eligible to travel internationallyPast experience in an Event Agency, PCO, or other event-related position is a plus.SpotMe recruits, compensates, and promotes regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, parental status, or veteran status.

IT Healthcare Project & Support Engineer (m/w/d) International Heidelberg Engineering GmbH u2022 Heidelberg Vollzeit Heidelberg ab sofort Aufgaben2nd & 3rd Level Remote-Unterstützung unserer weltweiten Niederlassungen und Händler bei Projekten und Troubleshooting als HauptansprechpartnerUnterstützung bei der Verbesserung und Entwicklung unserer ProdukteEigenständige Bearbeitung von Serviceanfragen sowie das Qualifizieren, Dokumentieren und Priorisieren von StörungsmeldungenInstallation und Konfiguration notwendiger Client-Server Software-Komponenten per FernzugangDokumentation gemeldeter Probleme und Anfragen in unserem TicketsystemUnterstützung unserer Fachabteilungen, Schnittstellenfunktion zwischen FachbereichenTraining unserer Partner und Niederlassungen remote und in Heidelberg QualifikationenErfolgreich abgeschlossene Berufsausbildung oder Bachelor-Abschluss mit IT-Fokus (Berufseinsteiger möglich)Sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift notwendigErste berufliche Erfahrung im Bereich Informationstechnologie, z.B. im 2nd Level IT-Support, als Systemadministrator oder im IT-Service wünschenswertKenntnisse innerhalb von Windows Netzwerkadministration sowie im Virtualisierungsumfeld ProfilHohe soziale Kompetenz sowie eine gute KommunikationsfähigkeitAuch in stressigen Momenten behalten Sie den Überblick und Ihre Neugier und Ausdauer bringt Sie zu neuen LösungswegenSehr gute analytische FähigkeitenAusgeprägte Service- und TeamorientierungSorgfältige und zuverlässige ArbeitsweiseHohes Verantwortungsbewusstsein Wir bietenDich erwartet ein vielfältiges und abwechslungsreiches Aufgabengebiet Ein hochmotiviertes Team in einem internationalen Umfeld und einem familiären BetriebsklimaMöglichkeiten zum mobilen Arbeiten zur Vereinbarung der Work-Life-BalanceFlexible Arbeitszeiten und VertrauensarbeitszeitAttraktive, leistungsorientierte VergütungKostenzuschuss zum DeutschlandticketFirmenfahrrad zur privaten Nutzung im Rahmen eines Bikeleasing-AngebotsFitnesszuschuss für Pfitzenmeier, Venice Beach, FitBase und Urban Sports ClubBetriebliche AltersversorgungParkmöglichkeiten sowie FahrradkellerRegelmäßige MitarbeiterveranstaltungenBetriebliches Gesundheitsmanagement Unsere Benefits Betriebliche Altersvorsorge:Mit einem attraktiven und flexiblen Angebot unterstützen wir Sie bei der Altersvorsorge, sodass Sie gelassener der Zukunft entgegensehen können. Bikeleasing:Ob E-Bike oder City-Rad – erwerben Sie bei uns Ihr neues Firmenfahrrad – auch zur privaten Nutzung – im Rahmen unseres Bikeleasing Angebots. Damit unterstützen wir die globale CO2 Neutralität. Familienunternehmen:Unsere Unternehmenskultur bietet ein internationales Umfeld mit einem familiären Betriebsklima, in dem Sie sich mit Ihren Skills einbringen können. Feedbackgespräche:Eine konstruktive, reziproke und kontinuierliche Feedbackkultur sehen wir als wichtige Grundlage für Ihre nächsten Entwicklungs- und Karriereschritte. Sie trägt zu unserer offenen, transparenten und vertrauensvollen Unternehmenskultur bei und stellt somit ebenfalls einen unternehmerischen Erfolgsfaktor dar. Fort- und Weiterbildungsu00admöglichkeiten:Lebenslanges Lernen und kontinuierliches Weiterbilden gehört zu den Erfolgsfaktoren in dem dynamischen Umfeld, in dem wir agieren. Daher ermöglichen wir Ihnen Zugang zu unserer digitalen Lernplattform, sodass Sie jederzeit Ihre fachlichen, sozialen, methodischen und persönlichen Skills erweitern können. Frisches Obst und kostenfreie Getränke:Eine wöchentliche frische Obstlieferung und kostenfreie Getränke vor Ort bieten Ihnen einen guten Start in den Tag und versorgen Sie mit gesunder Energie. Auch dem Austausch mit Ihrem Team während der Kaffeepause steht dabei nichts entgegen. Halten Sie sich fit:Mit unserem Fitnesszuschuss für Pfitzenmeier, Venice Beach, FitBase und Urban Sports Club möchten wir Ihre Gesundheit unterstützen. Durch die Bandbreite an Fitnessstudios, Kursen und Standorten gibt es für Sie eine große Auswahl an Sportprogrammen. Jobticket:Sie sind mit den öffentlichen Verkehrsmitteln unterwegs? Gerne unterstützen wir Sie dabei mit unserem Zuschuss zum Jobticket und fördern dabei auch den ökologischen Gedanken. Jubilare:Zur Wertschätzung unserer Mitarbeitenden gibt es individuelle Aufmerksamkeiten zu Firmenjubiläen sowie Pensionierungen, um diese besonderen Anlässe zu würdigen. Mobiles Arbeiten:Wir bieten Möglichkeiten zum mobilen Arbeiten für mehr Work-Life-Integration und Flexibilität. Moderne Arbeitsbedingungen:Wir bieten flexible Arbeitszeiten auf Vertrauensbasis, 30 Tage Urlaub (auf Basis einer 5-Tage-Woche) sowie zusätzliche Sonderurlaubstage für besondere Anlässe. Onboarding Prozess:Für Ihren optimalen Start bei Heidelberg Engineering gestalten wir für Sie einen individuellen Einarbeitungsplan, sodass Ihrem erfolgreichen Onboarding nichts im Wege steht. ParkenOb mit dem Rad, Roller oder Auto – unsere kostenlosen Parkmöglichkeiten sowie ein separater Fahrradkeller in der Tiefgarage stehen für Sie zur Verfügung. Regelmäßige Mitarbeiterevents:Bei uns gibt es immer wieder Gelegenheiten, gemeinsame Erfolge zu feiern, wie zum Beispiel im Rahmen von jährlichen Sommer- und Winterfesten, auf Team-Events oder einfach mal so zum Afterwork-Treff. Top Lage:Unser attraktiver Standort in Heidelberg mit direkter Anbindung an die Autobahn, u00d6PNV und den Heidelberger Hauptbahnhof ermöglicht Ihnen eine schnellere sowie unkomplizierte Anreise. Corporate Benefits:Durch unseren kostenfreien Zugang zu unserer firmeneigenen Corporate Benefits Plattform können wir eine Vielzahl an Rabattierungen und über 800 Marken für unsere Mitarbeiter in den verschiedensten Kategorien, wie z.B. Kultur, Mode, Lebensmittel, Auto, Finanzen u.v.m. anbieten. Sie haben noch Fragen? Wir freuen uns auf Ihre Kontaktaufnahme!Kontaktieren Sie hier direkt unser Personalmanagement. Wir konnten Sie begeistern?Jetzt bewerben

Job Description (English below)COORDONNATEUR(TRICE), CONSTRUCTIONNous sommes présentement à la recherche d’un(e) Coordonnateur(trice) de construction dévoué(e), expérimenté(e) et motivé(e) afin de se joindre à notre mission d’accélérer la transition vers un avenir plus vert. Ce poste fait partie de notre audacieuse, passionnée et excellente équipe basée à Montréal, Québec. En vous joignant à notre équipe, vous jouerez un rôle clé dans l'établissement et la montée en puissance de nos opérations, et contribuerez à la construction de l'une des premières usines de batteries à grande échelle en Amérique du Nord. Ce rôle ne consiste pas seulement à gérer un chantier de construction; il s'agit de façonner l'avenir de l'énergie durable et de faire partie d'un parcours innovant dans le domaine de la production de batteries électriques. À propos du posteNous sommes à la recherche d’un(e) Coordonnateur(trice) de construction expérimenté(e) pour diriger et superviser un segment majeur de notre projet révolutionnaire de giga usine, axé sur la production de batteries électriques. Il s'agit d'un projet greenfield impliquant la construction d'une installation à la pointe de la technologie. Le projet est divisé en trois segments clés en aval, chacun nécessitant un Chef de projet de construction dédié. À propos de l'équipeVous travaillerez au sein d'une équipe de projet dynamique dédiée à l'achèvement réussi d'une installation de fabrication de haute technologie et de grande notoriété. Votre équipe sera composée d'assistants chefs de projet, de surintendants de chantier, d'ingénieurs, de responsables de la sécurité et de divers spécialistes de la construction. Vous collaborerez étroitement avec d'autres Chefs de projet de construction supervisant différents segments du projet, assurant ainsi la cohésion et la constance sur l'ensemble du projet. Principales responsabilités:Coordonner la planification et l'exécution du projet, en veillant à l'alignement avec les objectifs globaux du projet, les calendriers et les exigences opérationnelles. Diriger les opérations quotidiennes sur le chantier de construction, gérer le personnel et les sous-traitants de manière efficace. Allouer efficacement les ressources, y compris la main-d'œuvre, les matériaux et l'équipement, pour atteindre les jalons du projet. Assurer la conformité aux normes légales, aux règlements de sécurité et aux spécifications de qualité dans toutes les activités de construction. Maintenir une communication claire et constante avec toutes les parties prenantes du projet, y compris les clients, les architectes, les ingénieurs et les fournisseurs. Aborder de manière proactive et résoudre les problèmes ou retards du projet, en mettant en œuvre des plans de contingence efficaces. Superviser les aspects financiers du projet, y compris la budgétisation et le contrôle des coûts. Fournir des rapports réguliers sur l'avancement du projet à la direction et aux parties prenantes. Faire respecter des protocoles de sécurité stricts et promouvoir une culture de la sécurité sur le chantier. Diriger et motiver l'équipe du projet, en favorisant un environnement de travail collaboratif et productif. Northvolt est un employeur qui respecte l'égalité des chances; nous sommes un groupe d’individus diversifié, unis par une mission commune. Étant en expansion ultra rapide, nous offrons des opportunités de développement professionnel et d’aprentissage continu à l’interne. Veuillez s’il vous plaît postulez avec votre CV ou profil LinkedIn. ---------------------------- CONSTRUCTION COORDINATORWe are looking for a dedicated, experienced, and driven Construction Coordinator to join us in our mission to contribute to a greener future. The role is a key part of our passionate and excellent construction team based in Montreal, Quebec. By joining us, you will be a key player in ramping up operations and contributing to building one of the first large-scale North American battery factories. This role is not just about managing a construction site; it's about shaping the future of sustainable energy and being a part of an innovative journey in the field of electric battery production. About the jobWe are seeking an experienced Construction Coordinator to lead and oversee a major segment of our groundbreaking gigafactory project, which is focused on the production of electric batteries. This is a greenfield project involving the construction of a state-of-the-art facility. The project is divided into three key downstream segments, each requiring a dedicated Construction Project Manager. About the teamYou will be working as part of a dynamic project team dedicated to the successful completion of a high-profile, technologically advanced manufacturing facility. Your team will consist of assistant project managers, site superintendents, engineers, safety officers, and various construction specialists. You will collaborate closely with other Construction Project Managers overseeing different segments of the project, ensuring cohesion and consistency across the entire project. Key Responsibilities:Coordinate project planning and execution, ensuring alignment with the overall project goals, schedules, and operational requirements. Direct day-to-day operations on the construction site, managing staff and subcontractors efficiently. Efficiently allocate resources, including labor, materials, and equipment, to meet project milestones. Ensure compliance with legal standards, safety regulations, and quality specifications in all construction activities. Maintain clear and consistent communication with project stakeholders, including clients, architects, engineers, and vendors. Proactively address and resolve project issues or delays, implementing effective contingency plans. Oversee financial aspects of the project, including budgeting and cost control. Provide regular progress reports to senior management and stakeholders. Enforce strict safety protocols and foster a safety-first culture on the construction site. Lead and motivate the project team, promoting a collaborative and productive work environment.Northvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognize that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. Apply with your CV or LinkedIn profile.

Job Description We are looking for a driven Accommodation Coordinator to join us in our mission to contribute to a greener future. The role is a part of our excellent Construction team based in Skellefteå. Join us and become a part of a ramping up Northvolt Ett and contribute to building one of the first large scale European battery factories. About the jobThe construction site is one of the largest in Sweden, and your role is to coordinate the Contractors site facilities such as offices, canteen, locker rooms, and accommodation. You will be part of a team that works close together but it is also important that you can work independently. The days will be full of challenges and problem solving, which requires you to be structured and flexible. Since you will work close with the contractors on site, it is necessary to have good social skills and an ability to communicate in English. About the teamYou will work in a team of 4 people that handle seatings and accommodation for contractors at Northvolt Ett project in Skellefteå. The team is responsible for assigning seats, office and temporary accommodation for contractors - the success of the construction project depends heavily on the team. Key responsibilities include but are not limited to:Plan and organizeaccommodation for contractors.Contact person forcontractors at Site for seat assignment in temporary barracks/officesCollaborate cross functionalto make sure capacity for contractors are sufficientThe person we are looking for is flexible, curios and eager to learn. You will get the chance to contribute to our success story in Sweden (to start with) and see the results of your work. Our organization values great self-discipline and a natural talent to make things happen. Qualities that we cherish are sense of quality, friendliness, grit and a sense of humour. Apply with CV in English or your complete LinkedIn profile. Full time employment, fixed salary.Planned starting date as soon as possible.