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Global Clinical Research Manager
vor 3 Wochen
This role involves leading the development of clinical protocols, amendments, and other study-related documents, ensuring adherence to regulatory requirements.
Main Accountabilities:
- Support the clinical protocol development process, collaborating with Medical Leads and other line functions.
- Author clinical protocols, amendments, and other study-related documents.
- Contribute to the development of study-level regulatory documents.
- Develop strategic and scientific input into study concepts, feasibility, and execution.
Qualifications:
- Bachelor's degree in life science or healthcare; advanced degree preferred.
- Minimum 2+ years' experience in clinical trials/development.
- Excellent English communication skills.