Purpose of the role:
The successful candidate will review and design clinical protocols, monitor clinical trials, and communicate with international regulatory agencies. Position title is negotiable and will be commensurate to relevant experience.
Responsibilities:
- Critically review and revise clinical trial protocols
- Serve as primary communicator with Clinical Trial CRO providers and regulatory authorities
- Identify and communicate with local and international KOLs in therapeutic indications related to company programs
- Identify and engage with consultants and CROs for services related to company program
- Generate and make presentations on behalf of the company at external meetings and conferences
- Foster collaborative relationships with employees both within and outside the company
Technical requirements:
- Command a deep understanding of company programs and keep current with latest relevant scientific research and development
- Generation and review of technical reports and presentations
- Ability to search and survey the technical literature using online tools
Minimum qualifications:
- Doctor of Medicine (M.D.) or PhD in clinical sciences, or equivalent combination of education and experience
- Clinical trial experience in
oncology - Ability to communicate in written and spoken English and Chinese