Role Overview
The Global Development Lead will be responsible for progressing a molecularly targeted radiation therapy through clinical trials up to and including Phase 2. The role will be responsible for creating, implementing, managing and executing the drug development plan. The successful delivery of the development plan will require leading a cross-functional team (including manufacturing, non-clinical, clinical, quality and regulatory) and will need a strong understanding of oncology drug development.
What You Will Do
Work as part of a cross-functional team to create/manage a Target Product Profile and Product Development plan for the targeted therapy in solid tumours. Lead cross-functional teams to deliver the program development milestones up to the end of Phase 2 clinical evaluation within project timelines and budget.
Why It Might Be a Fit
Postgraduate qualifications in science or life sciences (ideally PhD) required. 10+ years’ pharmaceutical/biotechnology industry experience including direct experience in drug development (ideally in oncology) required. 3+ years’ project and budget management experience.
Requirements
- Postgraduate qualifications in science or life sciences (ideally PhD)
- 10+ years’ pharmaceutical/biotechnology industry experience including direct experience in drug development (ideally in oncology)
- 3+ years’ project and budget management experience
- An understanding of the regulatory environment in the US, EU and APAC pertaining to drug development
- Experience working as part of, and also managing, a cross-functional team
Benefits
- Competitive salaries
- Annual performance-based bonuses
- Equity-based incentive program
- Generous vacation
- Paid wellness days
- Support for learning and development
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