San Diego, South San FranciscoFull TimeHealthcare
Remotely
oncologydrug developmentclinical trialsregulatoryndakolindregistrational trials
Job Description
📋 Description
- Provide medical leadership and oversight of the lung cancer development program
- Collaborate with CMO across the Erasca portfolio; guide strategy and execution
- Lead protocol development, registrational strategy, and data-driven decision making
- Hands-on drug development; serve as clinical lead/medical monitor on studies
- Lead clinical subteams; monitor study integrity and safety/efficacy data
- Contribute to global regulatory filings and health authority interactions
🎯 Requirements
- M.D. degree with oncology/hematology board certification or eligibility; thoracic oncology
- 8-10+ years oncology clinical trial and drug development experience
- Experience leading late-stage lung cancer programs; regulatory filing involvement
- Strong collaboration in matrixed environments; executive leadership and stakeholder management
- Excellent communication/writing skills; ability to engage with thought leaders and regulatory bodies
- Knowledge of trial methodologies, endpoints, and regulatory standards
🎁 Benefits
- Base salary range: $390,000 to $435,000 per year
- Annual bonus and equity grants; stock purchase program
- Comprehensive benefits package (health, dental, vision, disability)
- 401(k) with Erasca contributions; employee stock purchase plan
- Flexibile PTO, holiday Leave, and wellness programs
