Überblick über die Statistik des Gehaltsniveaus für "International Contract Administrator 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

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

ScriptRunner Software GmbH, Ettlingen near Karlsruhe, offers the #1 Automation Solution for managing IT infrastructures with PowerShell. With our product, we make everyday life in IT operations easier for IT administrators and users from specialist departments. Our most important success factor is the intensive contact with our customers and partners as well as to the IT pro community in their ScriptRunner journey. As a fast-growing IT company (B2B) with international customers, we are innovative and offer you optimal career opportunities and further development possibilities. We are convinced that the combination of free development opportunities, passion and teamwork leads to innovative best performances. For our sales team we are looking for an Enterprise Account Manager – International (all gender) as soon as possible. Your tasks New customer acquisition up to contract conclusion in the enterprise segment (detailed pre-qualification through inbound marketing data available as well as modern outbound mechanisms) Expansion of cooperation with existing customers (actively pushing upselling- and renewal deals) Communicate the benefits of our automation solution to prospects and customers – focus on North America Working closely with our colleagues in the Customer Success team to provide optimal service to our customers Professional and convincing Pre-Sales product presentation Fun and pleasure in communicating in English - Native speaker preferred Your expertise Technical or commercial studies or comparable training At least 5 years of experience in IT Sales/Presales with customers from the larger midmarket/enterprise environment Good knowledge of the IT environment with a focus on IT infrastructures, IT operations and IT process knowhow Exceptionally good written and spoken English (and German) skills Your personality Customer and service-oriented way of thinking Distinct negotiation skills Excellent teamwork and communication skills High degree of willingness to learn and self-motivation Structured and independent way of working Presentation and enthusiasm skills Your working environment Flexible working hours, the opportunity to work mobile and workation Unique software solution with various USPs in the automation market Operating in a growth market with a promising future (IT automation) Well-known, satisfied customers in the enterprise segment Company is on a rapid growth course Highly automated sales/marketing processes for lead generation and lead development (nurturing In- and Outbound) Free development opportunities Fast decision making Standort ScriptRunner Software GmbH, Ettlingen

Enterprise Account Manager InternationalJob Location: Ettlingen, GermanyJob Type: Full TimeCareer Level: Senior LevelLanguages Requirement: English C1German C1Candidate Location Requirement: Based in Ettlingen, Germany.Work Experience:Enterprise Sales Manager [ 4 - 6 years ]Product Sales Manager [ 4 - 6 years ]Account Manager [ 4 - 6 years ]Sales Manager [ 4 - 6 years ]Skill- Set RequirementsSalesB2BSaaSCommunication SkillsSales ManagementAccount ManagementI.TDetailsLocated in Ettlingen near Karlsruhe, this organization provides the leading Automation Solution for IT infrastructure management using PowerShell. The product simplifies daily tasks for IT administrators and specialist department users. A key to success is the deep engagement with customers, partners, and the IT professional community throughout their journey with the solution. As an expanding B2B IT firm with a global client base, the company is at the forefront of innovation, offering excellent career growth and development opportunities. The belief here is that a mix of freedom in development, passion, and teamwork fosters groundbreaking achievements.For our sales team we are looking for an Enterprise Account Manager International (all gender) as soon as possible.Your tasksNew customer acquisition up to contract conclusion in the enterprise segment (detailed pre-qualification through inbound marketing data available as well as modern outbound mechanisms)Expansion of cooperation with existing customers (actively pushing upselling- and renewal deals)Communicate the benefits of our automation solution to prospects and customers focus on North AmericaWorking closely with our colleagues in the Customer Success team to provide optimal service to our customersProfessional and convincing Pre-Sales product presentationFun and pleasure in communicating in English - Native speaker preferredYour expertiseTechnical or commercial studies or comparable trainingAt least 5 years of experience in IT Sales/Presales with customers from the larger midmarket/enterprise environmentGood knowledge of the IT environment with a focus on IT infrastructures, IT operations and IT process knowhowExceptionally good written and spoken English (and German) skillsYour personality Customer and service-oriented way of thinkingDistinct negotiation skillsExcellent teamwork and communication skillsHigh degree of willingness to learn and self-motivationStructured and independent way of workingPresentation and enthusiasm skillsYour working environmentFlexible working hours, the opportunity to work mobile and workationUnique software solution with various USPs in the automation marketOperating in a growth market with a promising future (IT automation)Well-known, satisfied customers in the enterprise segmentCompany is on a rapid growth courseHighly automated sales/marketing processes for lead generation and lead development (nurturing In- and Outbound)Free development opportunitiesFast decision making Standort Talent Ocean, Ettlingen

Join our teamWe, ScriptRunner Software GmbH, located in Ettlingen near Karlsruhe, offer the #1 automation solution for managing IT infrastructures with PowerShell. With our product, we make daily operations easier for IT administrators and users from specialist departments. Our most important factor of success is the intensive contact with our customers and partners as well as the IT pro community on their ScriptRunner journey. For our sales team, we are looking for an Enterprise Account Manager – International (all genders) as soon as possible.You will be responsible for:New customer acquisition up to contract conclusion in the enterprise segment (detailed pre-qualification through inbound marketing data available as well as modern outbound mechanisms).Expansion of cooperation with existing customers (actively pushing upselling- and renewal deals).Communicate the benefits of our automation solution to prospects and customers – focus on North America.Working closely with our colleagues in the Customer Success team to provide optimal service to our customers.Professional and convincing Pre-Sales product presentation.Fun and pleasure in communicating in English - Proficient English skills.Your backgroundTechnical or commercial studies or comparable training.At least 5 years of experience in IT Sales/Presales with customers from the larger midmarket/enterprise environment.Good knowledge of the IT environment with a focus on IT infrastructures, IT operations, and IT process know-how.Exceptionally good written and spoken English (and German) skills.Customer and service-oriented way of thinking.Distinct negotiation skills.Excellent teamwork and communication skills.High degree of willingness to learn and self-motivation.Structured and independent way of working.Presentation and enthusiasm skills.This awaits you with usFlexible working hours, the opportunity to work mobile and workation.Unique software solution with various USPs in the automation market.Operating in a growth market with a promising future (IT automation).Well-known, satisfied customers in the enterprise segment.The company is on a rapid growth course.Highly automated sales/marketing processes for lead generation and lead development (nurturing In- and Outbound).Free development opportunities.Fast decision-making.More information on our website: https://lp.scriptrunner.com/en/jobs/enterprise-account-manager-international Standort ScriptRunner, Ettlingen

We are looking for you as Computer scientist / IT system administrator as technical buyer (m/f/d) software / IT to support our purchasing department with a technical background at the Mönchengladbach site. Scheidt & Bachmann you don't know? You certainly do! If you've ever taken the train, parked in a parking garage, paid at a petrol station or used a ticket machine, you've probably already come into contact with our products. We develop cutting-edge products and systems around the world to shape the mobility of the future. In our family of companies, values such as TRUST, RELIABILITY and COOPERATION are very important - and have been for more than 150 years. Together, we ensure that millions of people and goods around the world stay on the move and reach their destination quickly, easily and safely. We offer A permanent position in an innovative, crisis-proof and established company where diversity and equality are part of our DNA Work-life balance: look forward to flexible, family-oriented working hours, home office and part-time options and our childcare allowance Good food: Discover the varied range of food on offer in our modern company restaurant Structured induction and buddy system: We want you to feel comfortable right from the start and be able to contribute your know-how directly Personnel development and training programs: Develop yourself continuously to keep giving your team new impetus Lots of appreciation: attractive remuneration is just as important to us as working together as equals Your tasks Are negotiations your passion? You negotiate contracts and place orders, particularly in the product areas of \"software\" and \"hardware\". Do you have a structured way of working? You analyze service level agreements and license agreements from well-known software providers with the aim of finding the optimal procurement strategy. Do you enjoy project work? You support international internal and external IT infrastructure projects. Do you love efficiency? It's also your job to achieve more favorable purchasing conditions, terms and quality while observing value analysis principles. This will help you take your team to the next level. Reliability is your strength? You implement the requirements from our customer contracts. Are you sociable? You process complaints and clarify discrepancies in order confirmations or invoices. And are you also articulate? You correspond and communicate with internal and external interfaces in English and German. What you bring with you Successfully completed studies with a focus on business informatics, business law or business administration or completed vocational training as an IT systems clerk / IT clerk or industrial clerk (m/f/d) Ideally initial professional experience in IT purchasing / sales Good knowledge of the software and hardware segments Knowledge of contract law advantageous Good knowledge of MS Office, knowledge of SAP advantageous Business fluent in German and English Enjoy occasional business trips Assertiveness, ability to work in a team, independent way of working Communication and cooperation skills Are you interested? For further questions, please contact us: Frank Dohmen +49 2166 266-253 Career at Scheidt & Bachmann Career videos Apply now! If you are interested in joining our innovative family business, then apply now, stating your salary expectations. Scheidt & Bachmann GmbH - Breite Strau00dfe 132 - 41238 Mönchengladbach - Germany - karriere.scheidt-bachmann.de

An exciting and varied field of activity in an international environment with a high level of personal responsibility is exactly what you are looking for? Look no further, you've found the job! Our client, an internationally active industrial company in the Weil am Rhein area, is looking for an IT System Administrator with experience to join their team. The position is being offered on a full-time basis as part of a direct recruitment agency. Do you want to be the person? This position is to be filled as part of a direct placement / as part of a recruitment agency. IT System Administrator (m/f/d) with experience ID: 267312 Your tasks: Ensuring the daily operation (second and third level support) of the IT infrastructure on site and in the cloud, virtualization, servers, etc. with a focus on Microsoft-based solutions System configurations, integrations, licence management and performance optimization Infrastructure provision and design Proper documentation of the infrastructure environment and system administration activities Involvement in IT projects in relation to all infrastructure aspects Technical advice, support and monitoring Your qualifications: Completed vocational training in the IT environment with several years of professional experience in the field of activity described above Proven very good experience in the development, management and organization of infrastructures Strong expertise in Active Directory, Win 10, various servers, security implementations in mixed environments and experience with virtual environments (VMware) Technical understanding of databases, cloud technology (Azure, Office 365) and current network hardware, protocols and standards, including TCP/IP, Fast Ethernet etc. Fluency in written and spoken German and English Enjoy working in a team as well as independently, strong communication skills and a service-oriented approach Open-ended employment contract Flexible working hours and possibility of hybrid working Individual support Profit-sharing and capital-forming benefits and much more. With us, your career path will become your personal walk of fame - we offer you exciting prospects in the field of IT. Click on \"Apply directly\" now!

System Administrator - Infrastructure (m/f/d) Permanent position, full-time - Leipzig | HQ THIS IS US: SENEC has been one of the leading providers of innovative electricity storage and energy solutions for private households since 2009. As a wholly owned subsidiary of EnBW, we are one of the pioneers in the industry and are also active internationally with our headquarters in Leipzig and branches in Cologne, Milan and Bari. Together, we are creating a world in which everyone can generate, use and share their own renewable energy. Over 700 highly motivated employees work on this every day at SENEC. Would you like to be part of something really big? Is sustainability just as important to you as it is to us and do you want to revolutionize the future of energy supply with passion and commitment? Then we'd love you to join us as a System Administrator - Infrastructure (m/f/d) and help us make the world a better place! WHAT YOU CAN DO WITH US: You will be responsible for the support and further development of our on-premise IT infrastructure with a focus on network technology You are responsible for our server hardware, network components and backup systems You maintain our Microsoft Windows servers You ensure the system availability You monitor our systems with the help of our monitoring system You carry out error analyses and troubleshooting of various on-premise systems You are looking forward to working on projects to introduce new technologies and innovations You are the contact person for internal departments and work together with our global IT teams and external partners WHAT YOU COULD BRING TO US: Completed training in the field of computer science or a comparable degree Fluency in written and spoken German and English You can imagine working 2-3 days/week at the Leipzig HQ Experience in leading teams is an advantage WHAT YOU CAN LOOK FORWARD TO WITH US: We are shaping the Energiewende - combining the speed of a start-up with the security of our parent company EnBW. Become part of our dynamic, innovative and creative team with attractive benefits. You can expect: Competitive salary plus bonus Permanent employment contract with 30 days' vacation One-off home office allowance of 700 euros for all persons with a mobile employment contract Monthly child allowance of u20ac100 per child (max. u20ac200) Monthly allowance of u20ac30 for your public transport season ticket Flexible working hours, flexitime and, if the position allows, mobile working Discounted membership at Urban Sports Free language learning courses with Babbel Bike leasing Numerous offers via Benefits.me Individual team events Drinks, fruit and food allowance at the locations Varied tasks and room for personal initiative Strong willingness to make decisions and open error culture Authentic, motivated and enthusiastic team with a positive mindset Trusting collaboration across all departments and hierarchy levels HOW TO JOIN OUR TEAM: Please send your application to Nadia (HR Manager Recruiting). We look forward to receiving your informative CV, together with other documents such as a letter of motivation, references and certificates. If applicable, please also send us a copy of your residence permit and work permit. For better planning, please let us know your earliest possible start date or your notice period and your salary expectations. All people are welcome here, regardless of gender, age, sexual identity, origin, religion, ideology, with or without a disability. We look forward to getting to know YOU! ABOUT US We have been developing and producing intelligent electricity storage systems and storage-based energy solutions since 2009. We offer our customers maximum independence from external electricity suppliers with a complete range for self-supply with solar power. With more than 120,000 systems sold, SENEC is one of Europe's most popular brands for innovative energy and storage solutions. SENEC has repeatedly been recognized by EuPD Research as Top PV Brand Power Storage and Wallbox, most recently in 2022. Our SENEC.Home power storage system recently received the \"German Excellence Award 2020\" from the German Institute for Service Quality. Thanks to intelligent features such as the SENEC.Cloud and SENEC.Cloud To Go, our energy storage systems are among the most innovative and economical solutions on the market. SENEC has been a wholly owned subsidiary of EnBW Energie Baden-Wu00fcrttemberg AG since 2018. More than 700 employees currently work for us at the following locations Leipzig (international headquarters) Cologne Italy We are looking for people who are passionate and committed to contributing their versatile skills to the realization of innovative battery storage solutions and making our products even more powerful and attractive. Do you want to be part of something big? Is sustainability as important to you as it is to us? Do you want to revolutionize the future of energy supply? Then make the world a little better with us!

IT System Administrator (m/f/d) For our client, we are looking for an IT System Administrator (m/f/d) in the southwest of Munich at the earliest possible date The company is based in Munich and focuses on the development and production of specialized vehicles and system technology. The company offers international solutions and logistical support for various applications. Your tasks: Expansion, maintenance and management of the existing IT infrastructure Implementation, configuration and administration of Linux and Windows servers Provision, maintenance and servicing of software platforms and user tools Continuous further development and optimization of existing toolchains Monitoring and maintenance of active IT systems Installation and configuration of PCs as part of project work Your profile: Successfully completed studies in computer science, IT or comparable training Practical experience in server management for both Linux and Windows environments Very good programming skills in Python and Bash, as well as a sound understanding of common PC hardware and tools such as Gitlab, SVN, Debian and Jenkins Good written and spoken English skills Knowledge of the configuration of Windows 11 is desirable Our benefits for you: You will receive a permanent employment contract and have the chance of being taken on permanently by our client We offer inflation compensation payments of up to 2300 euros, vacation and Christmas bonuses in accordance with the IGZ collective agreement First bonus payment of 700 euros gross after 4 months and a further 700 euros gross after 14 months Possibility of a job ticket for the train (talk to us about it) Successfully recommend someone for the job and you will receive a promotion bonus of 500 euros We support flexible vacation planning so that you can achieve a good work-life balance Free work clothes are provided to ensure you are well equipped Have we piqued your interest? Then we look forward to receiving your application via our application form. Simply click on the \"APPLY NOW\" button. Do you know someone who fits the vacancy? Then get our referral bonus now! Get in touch with us right away by phone. We look forward to receiving your application!

Administrator Logistics (m/f/d) ID Logistics - develop an innovative future with us ID Logistics is a fast-growing, international logistics contract logistics service provider with a global turnover of 2.75 billion euros. ID Logistics operates almost 400 locations in 18 countries in Europe, North and South America, Asia and Africa and employs around 38,000 employees, up to 1,450 of them in Germany. With a balanced customer portfolio from trade, industry, detail picking, health care, FMCG and e-commerce - sector, ID Logistics offers its customers automated and innovative logistics solutions. We focus on sustainability in everything we do, equal opportunities and teamwork. For our newest logistics center in Hamburg we are with start 15.08.2024 in search of an experienced administrator Logistics (m/f/d). WHAT CAN YOU EXPECT? Creation of forecasts for effective corporate management Collection, analysis and communication of key performance indicators (KPIs) to evaluate company performance Creation of SOPs (Standard Operating Procedures) according to internal specifications Use of the internal administration dashboard to manage orders, stock levels and other relevant information On-site management of IT hardware, including installation, maintenance and troubleshooting Support with quality management processes, including documentation and improvement of processes WHAT DO YOU BRING TO THE TABLE? Completed commercial vocational training or a degree in logistics, supply chain management or similar Several years of professional experience in a similar position an advantage Ability to handle multiple requests and priorities simultaneously with a high degree of independence Experience in IT hardware management and high technical affinity Management experience an advantage Very good knowledge of German and good written and spoken English Strong communication skills YOUR OPPORTUNITIES: Very good development and promotion opportunities Exciting and varied areas of responsibility Numerous company benefits - such as a job bike and company pension scheme Working in a rapidly expanding company \"Turn friends into colleagues\" - Refer friends, acquaintances or former colleagues and receive up to u20ac1,000! Up to 30 days vacation per year Continuous personal development opportunities Flat hierarchies and short communication channels \"Open door mentality\"

The Deutsche Bundesbank is a special bank: an integral part of the European System of Central Banks with an important function in financial stability, banking supervision, monetary policy and payment transactions in Germany. Above all, however, we are a strong team of reliable and responsible people whose daily work also creates the technical IT conditions for a stable euro and other central bank tasks. Join us on the path to a digital central bank! IT trainees for our exciting IT qualification program Work location Frankfurt on the Main Working hours Full-time (part-time is possible in principle), fixed-term (initially for 2 years) Start date as of now Job ID 2024_0580_02 Do you already have knowledge of IT and want to develop into an IT specialist? With us, you have the opportunity to become part of a highly motivated team that ensures the smooth functioning of the client/server systems and network for European payment transactions. The Deutsche Bundesbank offers you a suitable and attractive qualification program in the IT area. Work of special value: your assignment with us Your tasks as a participant in the qualification program are varied. You will have the opportunity to apply theoretical knowledge directly in practice and expand your IT skills. During the program, you will be specifically prepared for your future tasks. After completing the qualification, you will support us in IT operations, analyze system and application statuses using state-of-the-art monitoring tools and develop solution concepts. You will have the opportunity to participate in European payment transactions and work on national and international IT projects. Special values: Your qualifications You have successfully completed vocational training in the IT sector (e.g. as a systems IT specialist, IT systems administrator) or in a similar field or have comparable knowledge from many years of professional experience Experience in incident and problem management is an advantage Willingness and health suitability to work different working hours (incl. on-call duty and some weekend assignments) Analytical skills, good time management, ability to work in a team, commitment and sense of responsibility Good written and spoken German and English skills We expect the willingness to undergo a security check in accordance with the Federal Security Clearance Act (Su00dcG). Valuable work deserves special benefits Remuneration & prospects international working environment, varied tasks, national and international exchange opportunities, your remuneration is 3,300 euros gross per month, after successful qualification a permanent employment contract is planned, with remuneration based on pay group 10 TVöD plus a bank bonus New Work Home office options, good technical equipment (e.g. smartphone, tablet, notebook), working hours: 39 hours/week, 30 days' vacation, promotion of compatibility of career and family/work-life balance Additional benefits Company health management, health and sports courses, company restaurant, free job ticket, central location Would you like to join our team? Then we look forward to receiving your application. If you have any questions in advance, simply get in touch with the relevant contact person. Your questions about the application will be answered by Zeynep Göru00fcken Tel. 069 9566 35728 [email protected] Your questions about the job will be answered by Ilona Stefanides Tel. 069 9566 36416 Please apply by 19.06.2024 with the job ID 2024_0580_02 via our online tool. Diversity and equal opportunities are important to us. Severely disabled people will be given preferential consideration if equally qualified. Part-time employment is generally possible. The Deutsche Bundesbank also promotes professional equality between women and men, particularly when filling management positions. We therefore particularly welcome applications from women. We welcome you in all your individuality! We look forward to getting to know you better with your application. You can find more information about the Bundesbank as an employer at www.bundesbank.de/karriere Deutsche Bundesbank | Wilhelm-Epstein-Strau00dfe 14 | 60431 Frankfurt am Main

Do you have an excellent understanding of IT systems? Would you also like to use your specialist knowledge to drive forward the IT processes of an innovative & international company in the pharmaceutical industry? Then this is the perfect opportunity for you! For the continuous growth of a renowned company, we are now looking for support in the administration of IT-based solutions in the Offenburg area. This position is full-time within the framework of direct recruitment. This position is to be filled within the framework of direct placement / within the framework of personnel placement. System administrator (m/f/d) in the pharmaceutical industry - ID: 282785 Your tasks: Further development, optimization and maintenance of MS Dynamics NAV Administration of users Support and integration of interfaces to MS Dynamics Internal point of contact for employees with support questions and training needs Execution of tests and quality assurance measures as well as documentation of processes Your qualifications: Completed training or studies in the field of computer science with initial professional experience in the above-mentioned areas of responsibility Initial knowledge in the field of administration & development using C/AL and SQL databases desirable Experience in the Dynamics NAV development environment advantageous Very good German and good written and spoken English skills Ability to work in a team and good communication skills as well as a strong service orientation Performance-oriented and independent way of working Salary: approx. 60,000-70,000 annual gross salary Permanent employment contract 30 days vacation Flexitime and option for hybrid working Company pension scheme & employer bonuses Individual training options The master plan for your career: We will find exactly the job that suits you. Click on \"Apply directly\" now!

IT Administrator (m/f/d) Position to be filled from:01.06.2024HERE YOU BRING YOURSELF IN Installation, configuration and maintenance of computers, peripherals, applications and network Administration of servers and applications Network administration (routing, switching, firewall) Error analysis in the event of hardware and software faults (1st and 2nd level support) Further development of IT security by developing and implementing security guidelines Collaboration on projects related to system technology, automation WHAT YOU BRING WITH YOU Completed vocational training with sound experience in the IT sector, e.g. as an IT specialist for system integration Very good knowledge of network technology and Windows / Linux servers Planning, administration and further development of the software infrastructure (MS365 solutions, cloud integration, ...) Good knowledge of software applications (ERP, CAD, DATEV, ) Programming knowledge VBA / Powershell / SQL / Javascript / Python an advantage, but not a requirement WHAT WE OFFER Attractive remuneration and permanent employment contract Varied area of responsibility with an international background Development and training opportunities in an industry of the future Team-oriented working atmosphere in a collegial environment Company pension scheme Bike leasing via job bike Corporate benefits Drinks on the house PersonnelConvince us. Send your complete application documents (with salary requirements and earliest possible starting date) as a PDF file to Anna-Lena Stork, [email protected] . She will also be happy to answer any further questions you may have on +49 6747 95388-0. We look forward to getting to know you. About usPYREG is a German manufacturer of carbonization systems for the upcycling of organic waste into high-quality COu2082-sequestering biochar (biochar) and regenerative heat As the market leader in the field of carbonization, PYREG has developed a patented pyrolysis technology that is characterized by its multi-material capability and individual control of the carbonization parameters. The PYREG Biochar is a \"Negative Emission Technology\" (NET). Left in the soil or used in other permanent material applications, this biochar creates a carbon sink. In this way, PYREG closes cycles and permanently removes carbon from the atmosphere (Biochar Carbon Removal (BCR)). The German CleanTech company was founded in 2009 as a spin-off of the TH Bingen, University of Applied Sciences. All PYREG plants are certified according to the EBC industry standard. At PYREG GmbH, we attach great importance to the sustainable and careful use of resources. All plant systems are manufactured at our company headquarters in Dörth. This enables us to guarantee that our systems really do deserve the \"Made in Germany\" seal of quality and always comply with the latest environmental standards.

Linux Administrator with focus on MySQL and SAMBA (m/f/d) Do you love to professionally operate Linux server systems in mixed environments (Mac/Windows/Linux) and your focus is on MySQL and SAMBA? We are Europe's leading partner for holistic product communication and are looking for you to join our IT operations team so that our customers can remain worry-free in the increasingly complex IT environment. What you can expect: You will be responsible for the administration and maintenance of our Linux server landscape. You manage and optimize MySQL databases. You take care of the setup, configuration and maintenance of SAMBA servers You ensure that all systems are available, secure and free of technical problems Performing backups and restores is your thing. Automation of recurring tasks using scripting (e.g. Bash, Python) You advise our customers on technical questions and problems as part of training courses Participation in IT projects and continuous further development of the IT infrastructure What you bring with you: You have successfully completed training or studies in the IT sector or a comparable qualification. Ideally, you have several years of professional experience as a Linux administrator Your strengths and in-depth knowledge are in the administration of MySQL and SAMBA. You are confident with shell scripting (Bash, Python an advantage). You have experience with network technologies and protocols as well as knowledge of implementing security measures at server level You are characterized by your ability to work in a team, strong communication skills and an independent way of working. Very good knowledge of German and English What you can look forward to: An appreciative working atmosphere in a professional, committed and successful team. Fair pay and exciting projects with well-known international customers from a wide range of industries with a high level of personal responsibility. A permanent contract and 30 days' vacation per year. Flexible working and opportunities for further training and development. Short decision-making processes and flat hierarchies. Numerous health and family benefits. If you are interested, please call us and/or send us your detailed application - by email to [email protected] - preferably stating your salary expectations and earliest possible starting date. If you have any questions or require further information, please contact our People and Culture team on 02564-919-0 or send an email to [email protected] ( https://www.laudert.com/karriere/stellenangebote/[email protected] ) . We are looking forward to hearing from you! Additional information: Requirements for the applicant: Advanced knowledge: MySQL database, bash, ksh, sh, csh (shell programming), Samba (Unix server for Microsoft clients) Expert knowledge: Linux operating system

Administrator Logistics (m/f/d) ID Logistics - develop an innovative future with us ID Logistics is a fast-growing, international contract logistics service provider with a global turnover of EUR 2.75 billion. ID Logistics operates almost 400 locations in 18 countries in Europe, North and South America, Asia and Africa and employs around 38,000 people, up to 1,450 of them in Germany. With a balanced customer portfolio from retail, industry, detailed order picking, healthcare, FMCG and the e-commerce sector, ID Logistics offers its customers automated and innovative logistics solutions. We focus on sustainability in our actions, equal opportunities and teamwork. For our newest logistics center in Hamburg we are looking for an experienced Logistics Administrator (m/f/d) to start on 15.08.2024. YOUR OPPORTUNITIES: Very good development and promotion opportunities Exciting and varied areas of responsibility Numerous company benefits - such as a job bike and company pension scheme Working in a rapidly expanding company \"Turn friends into colleagues\" - Refer friends, acquaintances or former colleagues and receive up to u20ac1,000! Up to 30 days vacation per year Continuous personal development opportunities Flat hierarchies and short communication channels \"Open door mentality\" WHAT CAN YOU EXPECT? Creation of forecasts for effective corporate management Collection, analysis and communication of key performance indicators (KPIs) to evaluate company performance Creation**** of SOPs (Standard Operating Procedures) according to internal specifications Use of the internal administration dashboard to manage orders, stock levels and other relevant information On-site management of IT hardware, including installation, maintenance and troubleshooting Support with quality management processes, including documentation and improvement of processes WHAT DO YOU BRING TO THE TABLE? Completed commercial vocational training or a degree in logistics, supply chain management or similar Several years of professional experience in a similar position an advantage Ability to handle multiple requests and priorities simultaneously with a high degree of independence Experience in IT hardware management and high technical affinity Management experience an advantage Very good knowledge of German and good written and spoken English Strong communication skills Additional information: Requirements for the applicant: Advanced knowledge: IT organization

IT System Engineer Server (m/f/d) Streck Transportges.mbH has its origins in the border triangle of Germany/France/Switzerland and has been successfully combining innovation with tradition for over 75 years. Today, Streck Transport is not only a leader, but also operates worldwide and has an excellent network of leading cooperations. As a medium-sized, owner-managed and international forwarding and logistics company, Streck Transport maintains its independence despite globalization. We are looking for a full-time Network Administrator (m/f/d) for our ITS department in Freiburg What you can expect Planning, installation and configuration of server systems Monitoring and maintenance of the IT infrastructure Analyzing malfunctions and carrying out troubleshooting Optimizing server performance and ensuring availability Implementing IT security guidelines and data protection requirements Documentation of system changes and configurations Communication with internal specialist departments and external service providers Participation in projects for the further development of the IT infrastructure What you bring with you Completed studies in computer science, business informatics or comparable training at a university, dual university or vocational academy Alternatively: Completed vocational training in the IT sector or comparable qualification Several years of professional experience in the field of IT systems engineering, ideally with a focus on server technologies Sound knowledge in the planning, installation and configuration of server systems Experience in the administration of Windows environments Good knowledge of network technologies Excellent German and good English skills as well as the temporary willingness to work on a project-related basis at various locations in Germany and Switzerland Confident handling of monitoring tools and IT security concepts Ability to work in a team, strong communication skills and independent working style What we offer you A future-proof job in a modern service company with a family atmosphere A permanent employment contract in an exciting and varied working environment 30 vacation days 38 hour week Social benefits such as company pension scheme and capital-forming benefits Option to work from home Health management through external fitness offers Job bike Further training and development opportunities Company social counseling Company parties Free hot and cold drinks Free parking facilities We would be delighted if you would like to make a difference with us.