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

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 automotive supply sector? 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 greater Black Forest 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. IT System Administrator - ID: 281253 Your tasks: Network administration of servers, clients and printers Support for active and passive network components Management of users and access rights Provision of first and second level support for employees and processing of inquiries using the IT ticket system Procurement and installation of hardware and software IT system support and assistance with CAx applications Your qualifications: Completed training or studies in the field of computer science with initial professional experience Experience with operating systems for end devices, virtual servers, storage solutions and database management systems (SQL, Oracle) Knowledge in the field of network architecture Very good written and spoken German and English skills Ability to work in a team and good communication skills Performance-oriented and independent way of working Salary range: approx. 60,000-70,000 annual gross salary Permanent employment contract 30 days vacation Company pension scheme The master plan for your career: We will find exactly the job that suits you. Click on \"Apply directly\" now!

Library Administrator (m/f/d) for Airbus As a dynamic and modern personnel service provider, we offer our many years of experience and our comprehensive market know-how in a wide range of different industries exciting positions with interesting and innovative companies. Benefit from from our national and international networks and take advantage of STRATO personal as your personal springboard. We offer you comprehensive support and take care of all the administrative processes relating to your application - for you, of course free of charge. STRATO personal GmbH Temporary employment/employment agency/outsourcing/head hunting/onsite Management Get started with us! We realize exciting projects with our renowned client Airbus Defense and Space and are looking for the next possible date a motivated employee for the position of \"Library Administrator\" (m/f/d). (Reference number 0773SU2023ADS) Your tasks: Library administration: Maintenance of the component library for Capital (electrics) creation and Maintenance of library circuit symbols in Capital (electrics) Detailed design: Creation and maintenance of electrical production documents, such as logical circuit and overview diagrams and parts lists Close collaboration with the relevant developers Carrying out plausibility checks on the circuit diagrams created Your profile: Completed studies in the field of electrical engineering, mechanical engineering or mechatronics with further training as a master craftsman with relevant experience At least three years of professional experience in the field of construction Detailed specialized knowledge in dealing with MS-Office CATIA V5 knowledge is required CHS CAPITAL Logic knowledge is desirable Business fluent German language skills Advanced knowledge of English Ability and willingness to familiarize yourself independently with new fields of work We offer you: Permanent employment contract above-tariff remuneration plus vacation and Christmas bonuses + performance bonuses Prospect of being taken on Company pension scheme with employer subsidy Employee referral program with attractive bonuses Personal, local support and advice Assumption of costs for work clothing and health checks Contribution to travel tickets, if applicable Flexible working hours and partly mobile working Innovative and leading companies such as Airbus Operations, Airbus Aerostructures, Airbus Defence & Space, Airbus Helicopters, Premium Aerotec (Airbus) and the aerospace supply industry Interested? Then please apply with your complete application documents (current CV and references from your last three professional positions). Please understand that your documents must consist of cannot be returned for organizational reasons. Therefore, please refrain from sending expensive folders and photos, and original documents. Please note that we will store your data in our IT system in accordance with the provisions of the Federal Data Protection Act or store it when you apply. With your application you agree to the electronic processing/storage of your data. The storage at any time.

Our client is a globally recognized machine manufacturer for the industrial processing of food. As a family business, it offers its employees a secure job, a very good working atmosphere and plenty of scope to take on responsible tasks. Here, everyone can get involved in their team and contribute to the realization of major international projects. JobChance 37-hour week and home office after induction from 54,000 euros Direct placement in a permanent position with the client IT System Administrator (m/f/d) in Creglingen Administration of client and server systems Ensuring the ongoing operation Administration of our internal network and IT landscape Carrying out fault analyses and responsible for troubleshooting Ensuring the security of all stored data (data backup) Collaboration in projects for requirements analysis and implementation of new systems Supporting the specialist departments with the installation and administration of required user software Inventory and monitoring of contract terms (e.g. CarePacks / maintenance contracts) Degree in computer science, completed IT training or equivalent experience Sound knowledge of Windows client-server systems Network knowledge and basic knowledge of databases (SQL, Oracle, ) Knowledge of Crystal reports and VBA programming an advantage Reliable and independent way of working Team orientation and a high willingness to learn and work hard Systematic, solution-oriented approach Open-minded and communicative demeanor 30 days vacation 37h week vacation pay Year-end bonus Special leave for personal events Individual health budget Employee offers - corporate benefits Company pension scheme with employer contribution Very good working atmosphere in a medium-sized family business Thorough induction and support from a competent team Performance-related promotion opportunities Long-term prospects and ongoing training Flat hierarchies and a high degree of personal responsibility Secure job in a successful environment

Are you an IT professional looking for a new challenge in a dynamic and international environment? That's perfect! We are looking for talented IT Administrators (m/f/d) for one of our renowned clients. An interesting career opportunity is currently available with one of our renowned clients as soon as possible in the field of IT administration as part of a direct placement in Sehnde. Your benefits: Attractive remuneration (between u20ac45,000 and u20ac55,000 depending on qualifications) Individual development and training opportunities Mobile working ...and much more! This position is to be filled as part of a direct placement / as part of a recruitment agency. IT Administrator (m/f/d) - hybrid working - (remote & presence) Your tasks: Supporting users in the Microsoft environment (MS Office, Windows, Active Directory) Configuring, installing and administering server systems and network components Performing daily data backups and system checks Providing first and second level support Trouble shooting and restoration of AD domain services Designing and operating corporate network infrastructures Acting as contact person for hardware and software problems Your qualifications: In-depth knowledge of MS Office / Office 365 and experience in working with Microsoft operating systems, Microsoft Exchange and network technologies Practical experience in the administration of ERP software is a plus Ability to work in a team and a strong hands-on mentality, paired with diligence and resilience Very good German and good English skills In 3 steps to 500u20ac: 1. find a candidate: Talk to someone you know who is interested in working for us. 2. send in the form: Fill out the recommendation form on our homepage 3. receive a cash bonus: You will receive u20ac250 after the recommended candidate starts their contract. After a successful probationary period, you will be paid a further u20ac250. With us, your career path becomes your personal walk of fame - we offer you exciting prospects in the IT sector. Click on \"Apply directly\" now!

Customer Support Engineer (m/f/d) for AIRBUS As a dynamic and modern personnel service provider, we offer our many years of experience and our comprehensive market know-how in a wide range of different industries exciting positions with interesting and innovative companies. Benefit from from our national and international networks and take advantage of STRATO personal as your personal springboard. We offer you comprehensive support and take care of all the administrative processes relating to your application - for you, of course free of charge. STRATO personal GmbH Temporary employment/employment agency/outsourcing/head hunting/onsite Management Get started with us! We realize exciting projects with our renowned client Airbus Secure Land Communication and are looking for the next possible possible date a motivated employee for the position of \"Customer Support Engineer\" (m/f/d). Your tasks: Responsibility for ensuring the defined operating status of a digital radio system with all network elements and applications Processing reported incidents and service requests, analyzing fault reports and solving technical problems via remote diagnosis or remote access or using test systems Working closely with on-site support, product development and subcontractors to restore and troubleshoot operational systems Your profile: Completed studies in the field of computer science or a comparable qualification Professional experience in the field of Linux administration RedHat Enterprise Linux Server and CentOS) desirable Knowledge in the field of Linux administration required Experience in working on complex project tasks Good knowledge of virtualization (VMware, vCenter, RedHat Enterprise Virtualization) Sound knowledge of network technology, TCP/IP, switching and routing Experience with SAN storage systems Very good knowledge of German and proficient in English Willingness to work in 3-shift operation We offer you: Permanent employment contract Above-tariff remuneration plus vacation and Christmas bonuses + performance bonuses Prospect of being taken on Company pension scheme with employer subsidy Employee referral program with attractive bonuses Personal, local support and advice Assumption of costs for work clothing and health checks Contribution to travel tickets, if applicable Flexible working hours and partly mobile working Innovative and leading companies such as Airbus Operations, Airbus Aerostructures, Airbus Defence & Space, Airbus Helicopters, Premium Aerotec (Airbus) and the aerospace supply industry Interested? Then please apply with your complete application documents (current CV and references from your last three professional positions). Please understand that your documents must consist of cannot be returned for organizational reasons. Therefore, please refrain from sending expensive folders and photos, and original documents. Please note that we will store your data in our IT system in accordance with the provisions of the Federal Data Protection Act or store it when you apply. With your application you agree to the electronic processing/storage of your data. The storage at any time.

Wir suchen dich als Informatiker / IT-Systemkaufmann als technischer Einku00e4ufer (m/w/d) Software / IT zur Unterstu00fctzung unseres Einkaufs mit technischem Background am Standort Mönchengladbach. Scheidt & Bachmann kennst du nicht? Und ob! Wenn du schon einmal mit der Bahn gefahren bist, in einem Parkhaus geparkt, an einer Tankstelle bezahlt oder einen Ticketautomaten benutzt hast, bist du mit hoher Wahrscheinlichkeit bereits mit unseren Produkten in Beru00fchrung gekommen. Weltweit entwickeln wir hochmoderne Produkte und Systeme und gestalten so die Mobilitu00e4t der Zukunft. In unserer Firmenfamilie werden Werte wie VERTRAUEN, VERLu00c4SSLICHKEIT und ZUSAMMENHALT grou00dfgeschrieben u2013 und das seit mehr als 150 Jahren. Gemeinsam sorgen wir dafu00fcr, dass Millionen von Menschen und Gu00fctern weltweit in Bewegung bleiben und schnell, einfach und sicher an ihr Ziel gelangen. Wir bieten Eine unbefristete Anstellung in einem innovativen, krisensicheren und etablierten Unternehmen, in dem Vielfalt und Gleichstellung zu unserer DNA gehören Work-Life-Balance: Freu dich auf eine flexible, familienorientierte Arbeitszeitgestaltung, Home-Office- und Teilzeitmöglichkeiten und unseren Kinderbetreuungszuschuss Gute Verpflegung: Entdecke das abwechslungsreiche Essensangebot in unserem modernen Betriebsrestaurant Strukturierte Einarbeitung und Buddy-System: Wir wollen, dass du dich von Beginn an wohlfu00fchlst und dein Know-how direkt einbringen kannst Personalentwicklungs- und Weiterbildungsprogramme: Entwickle dich kontinuierlich weiter, um deinem Team immer wieder neue Impulse zu geben Jede Menge Wertschu00e4tzung: Eine attraktive Vergu00fctung ist fu00fcr uns ebenso selbstverstu00e4ndlich wie ein kollegiales Miteinander auf Augenhöhe Deine Aufgaben Verhandlungen sind deine Leidenschaft? Du verhandelst Vertru00e4ge und fu00fchrst Bestellungen insbesondere aus den Produktbereichen u201eSoftwareu201c und u201eHardwareu201c durch. Du hast eine strukturierte Arbeitsweise? Du analysierst Service Level Agreements und Lizenzvertru00e4ge namhafter Software-Anbieter mit dem Ziel der optimalen Beschaffungsstrategie. Projektarbeit macht dir Spau00df? Du begleitest international interne sowie externe IT-Infrastrukturprojekte. Du liebst Effizienz? Deine Aufgabe ist es auch, gu00fcnstigere Einkaufsbedingungen, Konditionen und Qualitu00e4t unter Beachtung der wertanalytischen Grundsu00e4tze zu erzielen. Damit bringst du dein Team ein gutes Stu00fcck voran. Zuverlu00e4ssigkeit ist deine Stu00e4rke? Du setzt die Anforderungen aus unseren Kundenvertru00e4gen um. Du bist kontaktfreudig? Du bearbeitest Mu00e4ngelru00fcgen und klu00e4rst Abweichungen bei Auftragsbestu00e4tigungen oder Rechnungen. Und du bist auch noch sprachgewandt? Du korrespondierst und kommunizierst mit internen und externen Schnittstellen in englischer und deutscher Sprache. Das bringst du mit Erfolgreich abgeschlossenes Studium mit dem Schwerpunkt Wirtschaftsinformatik, Wirtschaftsrecht oder Betriebswirtschaftslehre oder eine abgeschlossene Berufsausbildung zum IT-Systemkaufmann / Informatikkaufmann oder Industriekaufmann (m/w/d) Idealerweise erste Berufserfahrung im IT Einkauf / Verkauf Gute Kenntnisse der Segmente Software und Hardware Kenntnisse des Vertragsrechtes vorteilhaft Gute Kenntnisse in MS Office, Kenntnisse in SAP vorteilhaft Deutsch- und Englischkenntnisse verhandlungssicher Spau00df an gelegentlichen Dienstreisen Durchsetzungsvermögen, Teamfu00e4higkeit, selbststu00e4ndige Arbeitsweise Kommunikations- und Kooperationsfu00e4higkeiten Hast du Interesse? Fu00fcr weitere Fragen kontaktiere: Frank Dohmen +49 2166 266-253 Karriere bei Scheidt & Bachmann Karriere-Videos Bewirb dich jetzt! Wenn es dich reizt, dich in unserem innovativen Familienunternehmen einzubringen, dann bewirb dich jetzt unter Angabe deiner Gehaltsvorstellung. Scheidt & Bachmann GmbH - Breite Strau00dfe 132 u2022 41238 Mönchengladbach u2022 Deutschland u2022 karriere.scheidt-bachmann.de

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!

Jun. IT service desk employee (f/m/d) Many good reasons for our customer In addition to fair and attractive remuneration, you will be offered the following additional benefits: Attractive remuneration Flat hierarchies - short decision-making paths Permanent employment contract Extensive induction period Regular further training Parking spaces available Flexible working hours What you can expect in your new job Our client, an internationally operating industrial company located in the French-speaking region, is looking for a committed Jun. IT service desk employee (f/m/d). As a Jun. IT Service Desk Employee (f/m/d) you are ready to take on new challenges and support our IT infrastructure. Provide first-line support to end users, including troubleshooting hardware and software issues as well as installation, configuration and maintenance of IT systems such as workstations and Windows servers (Active Directory, DNS, DHCP) Monitoring system performance with the aim of identifying and resolving potential problems and implementing preventive measures to ensure system stability Managing software applications within the Windows network, including deploying and managing IT hardware (e.g. laptops, phones) and assisting in the management of critical system infrastructure (e.g. backups, licenses) Creation and management of user accounts and access authorizations, including documentation of IT procedures and processes to ensure network and system security Working with senior system administrators on complex technical projects to promote an efficient and effective IT infrastructure What you bring with you University degree in information technology or a related field First professional experience as Jun. IT service desk employee (f/m/d) in the administration of Windows Server would be an advantage Sound knowledge of Windows Server and Workstation operating systems, including Active Directory, DNS and DHCP Experience with virtualization technologies, such as VMware or Hyper-V Excellent problem solving and communication skills. Language skills in English, French and/or German are an advantage. If you are looking for a challenging position in an international environment and meet the above requirements, we look forward to hearing from you. Your application Are you interested in the position Jun. IT service desk employee (f/m/d)? Then we should definitely get to know each other! The quickest way to contact us is via the \"Apply now\" button. We look forward to receiving your English CV. Do you have any questions in advance? Then give us a call, we will be happy to advise and support you in all phases of the job search. We look forward to receiving your online application as Jun. IT service desk employee (f/m/d)! Your contact person: abakus Personal GmbH & Co KG Thalkirchner Str. 1 80337 Munich Phone +49 89 2355540 The term \"employee\" and other personal designations used on this page are gender-independent. They are used exclusively for reasons of better readability.

For 20 years, we have been creating solutions for radiological image processing and diagnostics as the IMAGE group of companies in the heart of Rostock. We develop software for image viewing and diagnosis, image archiving and communication systems (PACS) and radiology information systems (RIS), which we sell internationally through our dealer network. To strengthen our team in Rostock, we are looking for the next possible date for a IT / System Administrator (m/f/d) With us you will ensure the smooth operation of our centrally managed hybrid Microsoft Exchange environment maintain and continuously develop the IT infrastructure and services for our departments (e.g. CRM, ticket management, Jenkins, GitLab, Redmine) - this includes the administration of some Linux servers or web servers with LAMP stack Error analysis and elimination with development of strategies for service improvement What you bring with you Good knowledge in the areas of Exchange, Active Directory as well as security concepts Knowledge of creating scripts and processes using Microsoft PowerShell Independent and structured way of working as well as quick comprehension for solving complex processes Service-oriented thinking and acting as well as enjoyment in dealing with people Good written and spoken German and English skills, as we work with an international team for international customers For applicants from abroad - willingness to relocate to Rostock/Germany Work permit/residence permit is available What makes us special A modern, familiar working atmosphere in the city center and close to the city harbor Contemporary break rooms, with everything that goes with it You are given creative freedom and personal responsibility in a growing market You can choose your own peripherals We customize your employment contract Up to 40 days vacation Working hours from 20 to 40 hours per week You work where you feel most comfortable - in the office or up to 50% in the home office (depending on the requirements of the position) We take care of your health Joint activities, such as running or bowling Health coaching sessions and health days Bike leasing Company supplementary health insurance We optimize your net salary with benefits such as remuneration in kind Pluxee Restaurant Pass Company pension scheme Capital-forming benefits We are an international team with colleagues from and on different continents and additional offices in the USA and India. Are you interested? Please send us your application documents, preferably in German and English, stating your salary expectations and possible starting date by e-mail to Katja Hoffmeyer (hr[]image-systems[dot]biz) Do you have any questions? Our HR manager will be happy to help: Ms. Katja Hoffmeyer IMAGE Information Systems Europe GmbH Lange Strau00dfe 16 | 18055 Rostock Phone: +49 381 496 58 20

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!

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.