💼 About This Role

You'll lead clinical science strategy for novel RAS-targeted oncology therapies in early-stage development. You'll drive the clinical development plan from phase 1 through regulatory submissions, directly impacting breakthrough therapies for patients with RAS-addicted cancers. This role offers high visibility and the chance to shape pivotal studies.

🎯 What You'll Do

• Lead clinical science aspects of the Clinical Development Plan strategy.
• Oversee medical/safety data reviews and study reporting.
• Design clinical trials and manage execution including site selection.
• Author regulatory briefing packs and respond to Health Authority questions.

📋 Requirements

• MD with oncology training preferred, and 5+ years in clinical development in pharma/biotech.
• Experience in trial design, protocol writing, and constructing CRFs.
• In-depth therapeutic area expertise in oncology and clinical trial experience.
• Strong knowledge of GCP, ICH, FDA, EMA guidelines and regulations.

✨ Nice to Have

• Early phase drug development experience.
• Experience mentoring other clinical scientists.
• Line management experience.

🎁 Benefits & Perks

• 🏖️ Flexible PTO
• 🏥 Comprehensive health insurance
• 📈 Equity grants
• 💼 401(k) matching
• 💡 Professional development opportunities

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 1 hour
3. 3Technical Presentation· 1 hour