Similar Jobs
See allNew Clinical Development Leader, Lifecycle Management
Praxis Precision Medicines
US
Clinical Development
Regulatory Strategy
Data Interpretation
Associate Director, Site Enablement – Oncology Delivery Unit
Partner Company
US
Clinical Operations
Oncology
Leadership
Executive Director, Lifecycle Lead
Kyverna Therapeutics
US
Drug Development
Clinical Development
Regulatory Affairs
Associate Director, Regulatory Affairs
Iovance Biotherapeutics
US
Regulatory Affairs
Cross-functional Leadership
Written Communication
Director, Medical Affairs Oncology, Strategic Evidence & Collaborations (SEC)
Gilead Sciences
US
Oncology
Medical Affairs
Strategic Planning
Key Responsibilities:
- Provide medical leadership for the lung cancer development program.
- Lead clinical study subteams and ensure trial integrity.
- Author regulatory documents and interact with health authorities.
Required Qualifications:
- M.D. with oncology fellowship and 8-10+ years of industry drug development experience.
- Proven experience in late-stage lung cancer clinical programs and regulatory submissions.
Compensation and Benefits:
- Salary range $390,000 - $435,000 plus annual bonus and equity.
- Comprehensive benefits including PTO, medical, dental, vision, 401(k), and more.
Erasca
Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for cancer patients. Its programs target the RAS/MAPK pathway, and it fosters a collaborative, mission-driven culture.