Clinical Study Coordinator
at eppdata GmbH
20253 Hamburg, Hoheluft-West, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 Dec, 2024 | Not Specified | 29 Sep, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
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Employment Type:
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Permanent | Independent - 1099 |
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Description:
WHAT YOU BRING ALONG
- Excellent communication and management skills
- Experience in research and medical trials as an investigator, study nurse, or CRA
- Knowledge of regulations and guidelines for clinical trials on human subjects
- Advanced knowledge in MS office
- Ability to develop and deliver both oral and written presentations
- Fluency in English at least upper intermediate or advanced (B2 - C1 level)
- Skills in statistical, technical, and database applications
ABOUT US
Eppdata GmbH is a growing service company offering information technology services for supporting clinical studies in the field of Neuroradiology with more than twenty internal employees. We are simplifying imaging data collection and use advanced data analytics and AI, accelerating patient access to new therapies and supporting the clinical study lifecycle.
We welcome individuals of all genders, nationalities, and backgrounds to join our team. Our goal is to bring together a group of talented individuals who can work collaboratively to make a positive impact on society through their work in the medical field. We are confident that you will find an international welcoming and supportive environment here, where your skills and expertise will be valued and your contributions will be meaningful
Responsibilities:
Coordination of study activities
- Track study initiation process, study operations and study closeout
- Prepare, review and update study documents
- Ensure training of all relevant entities on study-specific documents
- Image reading analysis, database quality assessment and quality checks
Direct communication with our international customers
- Demonstrate our processes and systems to potential customers
- Organize regular meetings with sponsors of your studies
- Manage requests and emerging issues from customers
- Collect information for improvement of our products
Intrateam collaboration
- Cooperate with other teams (e.g. IT Infrastructure, development, sales)
- Participate in the prioritization and refinement process for software development
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
20253 Hamburg, Germany