Related skills
leadership regulatory affairs clinical trials oncology medical affairs๐ Description
- Provide medical direction for late-stage programs and data-driven decisions.
- Lead late clinical development function, directly and through reports.
- Design and execute registrational trials in solid tumors.
- Serve as Medical lead on clinical programs and represent development teams.
- Develop clinical strategy, protocols, and regulatory milestones; liaise with KOLs.
- Maintain data-driven decision making and rigorous data review.
๐ฏ Requirements
- MD or equivalent with Oncology/Hematology board certification or eligibility.
- 12+ years oncology clinical trial and drug development experience.
- Experience leading medical affairs and global clinical development programs.
- Strong regulatory filing experience and health authority interactions.
- Excellent communication and leadership in matrix teams.
- Deep knowledge of trial methodology and regulatory compliance.
๐ Benefits
- Paid time off, holidays, and sick leave.
- Medical, dental, and vision plans.
- Disability and life/AD&D coverage.
- FSA/HSA options and commuter benefits.
- 401(k) with ER contributions; Employee Stock Purchase Plan.
- Pet insurance and employee assistance program.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Healthcare Jobs. Just set your
preferences and Job Copilot will do the rest โ finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!