Global Development Lead (Molecularly Targeted Radiation Therapy)
Key Accountabilities:
- Work as part of a cross-functional team to create/manage a Target Product Profile and Product Development plan for targeted therapy in solid tumours.
- Lead cross-functional teams to deliver program development milestones up to the end of Phase 2 clinical evaluation within timelines and budget.
- Serve as the primary point of contact for the program; maintain excellent internal and external communication.
- Provide oversight of a Project Manager to ensure application of project management best practices.
- Oversee delivery of product development plans, including:
- Maintain up-to-date documentation of product positioning and target product profile.
- Track progress vs. development plan; notify of delays and/or changes.
- Document and track program budget with Finance and the project manager to ensure accurate, timely contract/cost recording.
- Assess product development risks with senior management and compile risk mitigation/scenario plans.
- Conduct regular reviews of documentation, progress, scope, timelines, and budget.
- Keep program team and executive informed of status, costs, and risks.
- Support project managers with periodic reports to internal stakeholders (including senior management).
- Contribute to definition and delivery of corporate objectives; prepare timely and accurate management reports.
- Maintain current awareness of program-related scientific, clinical, and commercial knowledge.
- Represent the program team at internal and external meetings.
Education and Experience / Requirements:
- Postgraduate qualifications in science or life sciences (ideally PhD) required.
- 10+ years pharmaceutical/biotechnology industry experience with direct drug development experience (ideally oncology) required.
- 3+ years project and budget management experience.
- Understanding of regulatory environment in US, EU, and APAC.
- Experience working as part of, and managing, a cross-functional team.