29 Jobs für Clinical Data Coordinator
Stellenangebote Clinical Data Coordinator Jobs
Job vor 4 Tagen bei StepStone gefunden
Milteny GmbH
• Bergisch Gladbach
Homeoffice möglich
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical [. .. ] at all stages. As a Clinical Trial Assistant, you will be supporting the Clinical Trial Manager in all aspects that are required to keep the quality and timeliness of study data and communication on a high level: You support the distribution and tracking of critical clinical documents and information, e. g. essential documents, study supplies, budgets, manuals, other site and subject related information and investigational product releases in collaboration with the study team. Next this, you support the preparation and submission [. .. ] in internal team meetings, taking minutes and providing status updates. You have already gained experience in clinical research as a clinical trial associate, clinical research associate and/or clinical study coordinator in the pharmaceutical/ biotech industry and/or you are a holder of an academic degree in life sciences, natural sciences, or healthcare. Attention to detail comes naturally to you as well as being highly organized. You are are used to prioritize multiple tasks, to take initiative, to work independently and [. .. ]
Job vor 8 Tagen bei Jobware gefunden
TRB Chemedica AG
Produktmanager Healthcare (m/w/d) Marketing
• Feldkirchen bei München
Homeoffice möglich
30+ Urlaubstage
[. .. ] (m/w/d) Digital Marketing Manager Healthcare (m/w/d) Marketing Communications Manager Healthcare (m/w/d) Content Manager Healthcare/ Pharma (m/w/d) Commercial Product Specialist (m/w/d)
Clinical Product Manager (m/w/d) Medical Affairs Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (m/w/d) Scientific Product Specialist (m/w/d) Medical Science Liaison (m/w/d) (mit leichter Marketingnähe) Medical Content Specialist (m/w/d) Event Congress Manager Healthcare (m/w/d) Healthcare Communications Manager (m/w/d) Education Training Manager Medical Devices [. .. ] Manager Healthcare UX Content Manager Med Tech Healthcare E-Commerce Manager Digital Communications Manager Pharma Marketing Automation Specialist Healthcare Scientific Affairs Specialist Clinical Research Associate (mit Produktfokus) Medical Information Specialist Evidence Data Manager Healthcare Clinical Evidence Manager Med Tech Regulatory Product Communication Specialist Medical Event Manager Healthcare Training Coordinator Medical Congress Coordinator Education Specialist Medical Devices Health Communications Specialist Corporate Communications Manager Healthcare 71621652 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
JOIN US ON OUR EXCITING JOURNEY IQVIA is The Human
Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/ multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products [. .. ] g. , timelines, financial, process, resource Maintain strong customer relationships Ensure open communications with customer and Quintiles management to manage and meet contractual obligations Service Management Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders Support DM service delivery with comprehensive DM process and technical expertise in executing projects Serve [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
Quality Manager (Dosimetry Laboratory) (P3)
• Seibersdorf, Niederösterreich
[. .. ] techniques within a framework of quality assurance. The Dosimetry and Medical Radiation Physics Section (DMRP) is responsible for quality assurance and metrology in radiation medicine. The Section [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] works closely with clinical colleagues of the Applied Radiation Biology and Radiotherapy Section and the Nuclear Medicine and Diagnostic Imaging Section. Specifically, DMRP provides technical support in medical physics to ensure the safe and effective applications of nuclear technology in radiotherapy, diagnostic radiology and nuclear medicine. It operates the Dosimetry Laboratory located at the [. .. ] work, and mentors scientific visitors and IAEA DOL fellows in QMS procedures. Role The Quality Manager (Dosimetry Laboratory) is a technical specialist on dosimetry instrumentation, calibration and audit methodologies; a coordinator, developing, maintaining and improving the dosimetry laboratory integrated quality and safety management system; a collaborator, contributing to the DOL R D work; and a mentor for scientific visitors and IAEA fellows in dosimetry calibration and audit techniques, and QMS procedures. Functions/ Key Results Expected Coordinate the development, maintenance and implementation [. .. ] comparison plan. Coordinate with the relevant IAEA Officers the implementation of IAEA dosimetry comparisons. Contribute to the implementation of the DOL dosimetry auditing and calibration services including quality assurance of data processing and report preparation. Contribute to the DOL R D work, including testing and maintenance of dosimetry and instrumentation systems and developing new auditing procedures. Provide measurement support to coordinated research projects in dosimetry. Act as alternate Radiation Protection, Health and Safety Officer. Mentor scientific visitors and train IAEA fellows [. .. ]
Job am 27.11.2025 bei Jobleads gefunden
• Seibersdorf, Niederösterreich
[. .. ] techniques within a framework of quality assurance. The Dosimetry and Medical Radiation Physics Section (DMRP) is responsible for quality assurance and metrology in radiation medicine. The Section [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] works closely with clinical colleagues of the Applied Radiation Biology and Radiotherapy Section and the Nuclear Medicine and Diagnostic Imaging Section. Specifically, DMRP provides technical support in medical physics to ensure the safe and effective applications of nuclear technology in radiotherapy, diagnostic radiology and nuclear medicine. It operates the Dosimetry Laboratory located at the [. .. ] work, and mentors scientific visitors and IAEA DOL fellows in QMS procedures. Role The Quality Manager (Dosimetry Laboratory) is: a technical specialist on dosimetry instrumentation, calibration and audit methodologies; a coordinator, developing, maintaining and improving the dosimetry laboratory integrated quality and safety management system; a collaborator, contributing to the DOL R D work; a mentor for scientific visitors and IAEA fellows in dosimetry calibration and audit techniques, and QMS procedures. Functions/ Key Results Expected Coordinate the development, maintenance and implementation of [. .. ] comparison plan. Coordinate with the relevant IAEA Officers the implementation of IAEA dosimetry comparisons. Contribute to the implementation of the DOL dosimetry auditing and calibration services including quality assurance of data processing and report preparation. Contribute to the DOL R; D work, including testing and maintenance of dosimetry and instrumentation systems and developing new auditing procedures. Provide measurement support to coordinated research projects in dosimetry. Act as alternate Radiation Protection, Health and Safety Officer. Mentor scientific visitors and train IAEA fellows [. .. ]
Job am 22.11.2025 bei Jobleads gefunden
Team Leader-Relationships
Führungs-/ Leitungspositionen
[. .. ] key function that powers Trilogys expansion and industry leadership. You will act as the trusted voice of the partner both across our organisation and throughout the sector. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] With access to data, systems, and senior leadership backing, you will take ownership for: Building and leading a high-performing Relationship team. Embedding Trilogys values of Value, Choice, and Make it Easy through every partner interaction. Developing strategy and structures that make Trilogy the most compelling partner for industry collaboration. Driving deeper engagement, satisfaction, and outcomes from our national partner network. What Youll Drive Client growth via Trilogys care coordinator and service provider relationships. Systems and processes that strengthen our role as a trusted contributor to partner success. A communication and engagement framework that keeps partners informed and connected to our mission. Partner enablement through training, support materials, and service insights. Cross-functional collaboration with Care, Clinical, Sales, Compliance, Operations, and Finance. Continuous improvement initiatives that remove friction and deliver measurable partner value. Contribution to referral growth, retention, and revenue performance, backed by clear KPIs and analytics. What Youll Bring Minimum two years experience leading or managing a team. Strong background in account management, business development, or [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] review, approval, and implementation of medical and commercial materials. You will be product or project business lead for global CMRP at Takeda CMRP Meeting Chair-pausing to communicate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping team focus on our ultimate stakeholders which are the patients who trust us to do the right thing, and overseeing escalation steps if MLR cannot come to alignment or if there is new data or campaigns that require senior level management input or alignment. Strategic business partner from clinical trial development through the marketing maintenance phase of a product lifecycle Subject matter expert on EFPIA, IFPMA, and FDA code/ regs, guidance, industry standards, complaints/ violations, and innovative promotional platforms Act as a strategic partner spanning clinical trial development through the marketing and maintenance phases of the product lifecycle. Regulatory [. .. ]
Job am 26.10.2025 bei Jobleads gefunden
Special Operations Physical Therapist (Baumholder, Germany)
• Stuttgart, Baden- Württemberg
[. .. ] injections, and referrals to specialty providers. Directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer within their scope of practice as directed by the HP [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Program Manager/ Coordinator. Participate in periodic meetings with HP and POTFF to review patient care and identify improvement opportunities. Serve as an advisor on sports medicine, injury prevention, rehabilitation, and human performance research for the HP Program Manager/ Coordinator. Serve as an advisor for administrative matters, purchasing supplies, equipment, and supplemental fiscal requests. [. .. ] for HP staff as directed by governing credentialing bodies and local medical oversight processes. Assist in developing and updating criteriabased job descriptions and performance standards. Assist in developing and maintaining clinical practice guidelines across HP Training Centers and associated facilities. Assist with short and longterm fiscal planning and submit input to the HP Program Manager/ Coordinator. Attend and participate in meetings with other POTFF staff and medical providers as required. Ensure safe and effective operation of patientcare equipment and contribute to [. .. ] (e. g. , AHLTA, MHS GENESIS) and/or HP Enterprisewide database (e. g. , Smartbase) as required by DODI 6040.45 and HP program directives. Collect and report all requested data to the HP Program Manager/ Coordinator and USSOCOM HQ/ its POTFF staff. Proficiently utilize computers, software, and technologies as required for the HP program. Perform other tasks within the scope of the PT position as assigned. Required Education/ Experience/ Skills/ Training U. S. Citizenship. Secret or Top Secret Clearance, or [. .. ]
Job am 14.10.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium
Betriebliche Altersvorsorge
[. .. ] chances of interviewing at BONAGO Incentive Marketing Group by 2x Get notified about new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Tester for a car voice assistant project-English (Australian) speaker Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Supply Chain Project Coordinator (m/f/d) Product Process Support Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Junior Projektmanager Elektrotechnik (all gender) Working Student Smart Site Operations Strategy (m/f/d) Intern Sustainability Management (f/m/d) Working Student Medical ML Data Management (f/m/x) Project Manager-Employee Research/ Surveys Tester for a car voice assistant project-French (France) speaker Strategic Project Assistant to CSMO (m/w/d) Working Student: Product Management and Data Analyst Associate (f/m/div) Were unlocking community knowledge in a new way. Experts add insights directly [. .. ]
Job am 26.09.2025 bei Jobleads gefunden
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Essen, Nordrhein- Westfalen
Overview Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 20.09.2025 bei Jobleads gefunden
Clinical Research Associate (Home-Based) - Clinical Research
Coordinator Experience Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 28.08.2025 bei Jobleads gefunden
Projektmitarbeiter der Geschäftsführung (all genders) Vollzeit in München
• München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium
[. .. ] Get notified about new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) Tester for a car voice assistant project-English (Australian) speaker Team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Supply Chain Project Coordinator (m/f/d) Product Process Support Greater Munich Metropolitan Area 4 weeks ago Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Hallbergmoos, Bavaria, Germany 1 month ago Client Success Project Business Coordinator (m/f/x) Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Working Student Smart Site Operations Strategy (m/f/d) Junior Projektmanager Elektrotechnik (all gender) Project Manager-Employee Research/ Surveys Working Student: Product Management and Data Analyst Associate (f/m/div) Tester for a car voice assistant project-French (France) speaker Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 60156860 [. .. ]
Job am 03.07.2025 bei Jobleads gefunden
• Hamburg
Field
Data Collection Specialist Surveyor Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Field Data Collection Specialist Surveyor 9 months ago Be among [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the first 25 applicants Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Company description: Terry Soot Management [. .. ] Management and Manufacturing Industries Outsourcing and Offshoring Consulting Referrals increase your chances of interviewing at TSMG Holding by 2x Sign in to set job alerts for Field Specialist roles. Field Clinical Specialist, Transcatheter Mitral Tricuspid Therapies OEM Field Support Integration Engineer Talent Pool: Field Service Engineer/ Technician (d/f/m) for Diagnostics and Life Sciences in DACH region Field Technical Engineer/ Applikationsspezialist (w/m/d) Elektrophysiologie-Region Hamburg/ Hannover Learning and Development Specialist (all genders) Sales Operations Field Force Coordinator (gn) Field Clinical Specialist Central Lower Saxony-Nurse Biomedical Full time/ Part time Account Leader Energy Resources (w/m/d) Clinical Specialist (m/w/d) VELYS Robotics-Location: Hessen/ NRW Technical Training Program Developer Wind Turbines (d/w/m) Zoiss Engineering Gmb H Senior Compensation Benefits Specialist (all genders) Claims Restructuring [. .. ]
Job vor 6 Tagen bei Neuvoo.com gefunden
Rapid Trials
Clinical Research Coordinator (Part-time, On-site, Independent Contractor)
• Chemnitz
POSITION SUMMARY Rapid Trials is hiring an experienced
Clinical Research
Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] This part-time, freelance role is based in Chemnitz, Germany. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, and ensuring compliance with protocol, GDPR, and site SOPs. Location: On-[. .. ] Fibroscan, biopsy, EGD) Send appointment reminders Organize transportationand follow-up Request/ track medical records Share results with referral sources Coordinate with CRC Complete Sponsor or CRO logs Documentation Systems Enter data into EDC Review and QC data in EDC Compliance Training Complete onboarding requirements: Training on protocol and study-related tools and systems Site Training, including SOPs and workflow Ensure GDPR-compliant data handling, including consent for background checks and data usage EU work authorization and freelancer eligibility (tax ID, self-[. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
Miltenyi Biomedicine
Clinical Trial Assistant (m f d)
• Bergisch Gladbach, North Rhine- Westphalia
[. .. ] Description Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical [. .. ] stages. Job Description As a Clinical Trial Assistant, you will be supporting the Clinical Trial Manager in all aspects that are required to keep the quality and timeliness of study data and communication on a high level: You support the distribution and tracking of critical clinical documents and information, e. g. essential documents, study supplies, budgets, manuals, other site and subject related information and investigational product releases in collaboration with the study team. Next this, you support the preparation and submission [. .. ] internal team meetings, taking minutes and providing status updates. Qualifications You have already gained experience in clinical research as a clinical trial associate, clinical research associate and/or clinical study coordinator in the pharmaceutical/ biotech industry and/or you are a holder of an academic degree in life sciences, natural sciences, or healthcare. Attention to detail comes naturally to you as well as being highly organized. You are are used to prioritize multiple tasks, to take initiative, to work independently and [. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
IQVIA
Global Clinical Trial Coordinator (m/w/d) , German Speaking, Home-Office in DACH
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of early clinical trials. Joining our team offers the opportunity [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, ensuring compliance with regulatory standards and internal processes. [. .. ] role combines operational and administrative responsibilities and requires close collaboration with internal and external stakeholders. We currently offer an exciting opportunity to join the FSP team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany, Austria and Switzerland. RESPONSIBILITIES Coordinate clinical trials in early clinical development for both Sponsor and Study site. Support Clinical Trial Leaders, Clinical Trial Managers, Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation, conduct, close-out) . Prepare and manage clinical trial documentation Compilation and collection of submission documents. Maintain trial-specific data and timelines in electronic systems. Communicate effectively with internal and external partners (e. g. , statisticians, data managers, regulatory affairs, investigators) . Organize and monitor study-related activities, meetings, and documentation. Ensure timely preparation of submission documents for authorities and ethics committees. Manage essential documents for Investigator Site File (ISF) [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
GULP experts united
• Hamburg
[. .. ] being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits Your tasks Management of the Teamcenter [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] software for study data and documentation Booking test rooms and scheduling test subjects Procurement and provision of study materials and equipment Carrying out the studies: Application of products to subjects skin according to study requirements Carrying out measurements and other tests to evaluate the skin care products Ensuring compliance with safety and ethical guidelines [. .. ] the antiperspirant effect under warm conditions Your profile Completed training or studies in the field of natural sciences, cosmetic sciences or a related field Experience in conducting volunteer studies or clinical trials, ideally in the field of skin care or cosmetics Good knowledge in the use of database software and Microsoft Office applications Willingness to be present during ongoing studies Very good written and spoken German and English skills Careful way of working and attention to detail Team and communication skills [. .. ]
Job am 27.11.2025 bei Neuvoo gefunden
AMBOSS
Marketing Engagement Coordinator (US Clinicians)
• Berlin
[. .. ] are AMBOSS and we are looking for a Marketing Sales Representative to join our team, and shape the future of medical education with us About AMBOSSAMBOSS is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a dynamic learning and clinical decision support tool committed to empowering physicians globally to deliver optimal care. Since our inception in, weve harnessed cutting-edge technology to transform the way physicians acquire and apply scientific knowledge. Each AMBOS Sian is passionate about being the champion of clinicians today-this motivates and unites us each day [. .. ] platform. Assist in managing residency program group discounts, including communicating with interested residents, tracking participation, and ensuring timely delivery of materials or follow-ups. Collaborate with cross-functional teamsincluding Marketing, Data Analytics, Customer Support, and the U. S. Students Commercial teamto align outreach efforts and share learnings. Analyze engagement data and user feedback to evaluate the success of initiatives and identify opportunities to improve future events and campaigns. Contribute to new outreach experiments, bringing creativity and initiative to test new formats, [. .. ]
Job am 24.11.2025 bei Neuvoo.com gefunden
R D Partners
• Aachen
Join us as a
Clinical Research
Coordinator in Aachen and help shape the future of clinical development-freelance flexibility, hospital-based impact. R D Partners is seeking a Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Coordinator to join a hospital site in Germany, on a freelancing basis. This role offers an exciting opportunity to contribute to clinical development within a CRO environment. [. .. ] Employment Agency in relation to this vacancy. By submitting this application, you confirm that youve read and understood our privacy policy, which informs you how we process and safeguard your data-https:/ / 70417157 [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Frankfurt
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Düsseldorf
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Munich
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Cologne
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Berlin
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Stuttgart
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]
1 von 2Weiter » Weitere Suchergebnisse laden »
Häufig gestellte Fragen
Wieviel verdient man als Clinical Data Coordinator pro Jahr?
Als Clinical Data Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 29 offene Stellenanzeigen für Clinical Data Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Clinical Data Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Coordinator Stellenangebote:
- Medpace (9 Jobs)
- TRB Chemedica AG (2 Jobs)
- Milteny GmbH (1 Job)
- Rapid Trials (1 Job)
- Miltenyi Biomedicine (1 Job)
- IQVIA (1 Job)
In welchen Bundesländern werden die meisten Clinical Data Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Coordinator Jobs werden derzeit in Nordrhein-Westfalen (6 Jobs), Hamburg (3 Jobs) und Berlin (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Coordinator Jobs?
Clinical Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
