Offer summary
Qualifications:
MD or equivalent required, Postgraduate training in TA or related specialty preferred, 4+ years industrial experience required, Ability to travel up to 20% domestically and internationally.
Key responsabilities:
- Serve as primary medical oversight for clinical trials
- Manage Phase 1-3 studies with decision-making responsibilities
- Provide medical expertise to internal and external teams
- Lead Clinical Development Plan execution and protocol consistency
- Contribute to regulatory documents and training sessions