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program management gcp clinical trials oncology cro📋 Description
- Lead strategic planning and execution of oncology clinical trials (Natera-sponsored interventional studies).
- Oversee feasibility, enrollment modeling, timelines, and budget.
- Collaborate with Clinical Development, Regulatory, Medical Affairs, Biostatistics, Oncology Product, and Commercial.
- Manage CRO partnerships, cross-functional teams, and data quality for regulatory and commercial goals.
- Ensure studies run efficiently, predictably, with strong operational rigor.
- Lead site activation and enrollment optimization; establish governance for trials.
🎯 Requirements
- Degree in relevant scientific discipline; advanced degree (MS, PharmD, MD, PhD) preferred.
- 10+ years in clinical research with 5+ years leading trials.
- Extensive global CRO leadership experience with governance frameworks and enterprise oversight.
- Experience managing all aspects of clinical trials: design, protocol, site monitoring, and recruitment.
- Extensive oncology trial program oversight; knowledge of FDA/EMEA Regulations and GCPs.
- Willingness to travel up to 25%.
🎁 Benefits
- Annual performance incentive bonus.
- Long-term equity awards.
- Comprehensive health benefits (medical, dental, vision).
- 401(k) with company match.
- Generous paid time off and company holidays.
- Additional wellness and work-life benefits.
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