- To support the Medical Director, as and when necessary.
- To ensure that the medical activities of the unit conform to industry standards and regulatory requirements.
- To provide business development support by meeting with sponsors and assisting in feasibility activities.
- To assist Physicians in the clinical studies performed in the unit.
- To liaise with Sponsors during protocol development, regarding aspects of protocols such as design and safety and provide input into dose escalation discussions.
- Appropriate experience in clinical pharmacology in early phase I/II studies.
To be considered for this opportunity please send your CV to Marija Petrovic at firstname.lastname@example.org