Related skills
gcp oncology mrd biomarker-driven📋 Description
- Serve as program-level medical lead for MRD oncology trials; ensure patient safety.
- Define development strategies aligning design, endpoints, and regulatory objectives.
- Provide medical oversight from trial design to first patient in and data readout.
- Offer cross-functional leadership with Clinical Science, Operations, Data, and Biostatistics.
- Act as Medical Monitor: safety signal detection and risk mitigation per GCP.
- Represent Natera to investigators, key opinion leaders, IRBs, and regulators.
🎯 Requirements
- MD (or equivalent)
- >=3 years oncology clinical development experience.
- Medical Monitor or clinical lead for Phase II-III trials.
- Strong knowledge of GCP, ICH guidelines, regulatory expectations.
- Proven ability to interpret and communicate complex clinical data.
🎁 Benefits
- Competitive benefits: medical, dental, vision, life and disability.
- Free testing for employees and dependents; fertility care benefits.
- Pregnancy and baby bonding leave; 401k benefits; commuter benefits.
- Generous employee referral program.
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