Principal Scientist overseeing clinical program execution at a bio - pharmaceutical company. Leading cross - functional teams in clinical development activities from strategic planning to post - marketing approval.
About the role
- Clinical Project Manager coordinating clinical studies and managing project teams across multiple locations. Engaging with international clients on complex clinical research initiatives.
Responsibilities
- Independent and accountable project planning and end-to-end project execution
- Coordination of the project team across multiple functional units and countries
- Primary contact for the client
- Oversight of global vendor management (partner CROs)
- Training and support of the project support team
Requirements
- Degree in a natural science or comparable qualification, preferably with a medical focus
- 1–3 years' experience in clinical research, monitoring, or in a project management role
- Experience with non-interventional studies (NIS) and academic clinical trials
- Good knowledge of GCP/ICH, ISO 14155 and ISO 20916, as well as AMG/MDR/IVDR
- Proficient in Microsoft Office applications
Benefits
- 30 days annual leave (based on a 5-day work week)
- Flexible working hours
- Overtime compensation or time-off in lieu
- Option to work from home up to three days per week (60:40 model)
- Company bicycle (bike leasing)
- VWL (capital-forming payments / employer savings contributions)
- Additional allowance for health promotion
- Regular company events
- Team-building events
- Learning and development opportunities (e.g., Babbel app)
- Complimentary electric car charging stations
- Complimentary fruit basket and drinks flat rate
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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