Senior Director, Oncology Clinical Trial Operations

Natera

San Carlos, CA, United States
**
Oncology clinical trial execution
Cro selection and oversight
Gcp compliance and inspection readiness
** Natera is seeking a Senior Director for Oncology Clinical Trial Operations in San Carlos, CA, to lead the strategic planning and execution of oncology clinical trials. The ideal candidate will have extensive experience in clinical research, particularly in oncology, and will be responsible for overseeing trial operations, managing CRO relationships, and ensuring compliance with regulatory standards. **

Job Summary

  • Lead the strategic planning and operational execution of oncology clinical trials evaluating Natera’s oncology products.
  • Responsible for feasibility assessment, enrollment modeling, timeline forecasting, budget development, and end-to-end study execution.
  • Serve as a key operational partner across Clinical Development, Regulatory, Medical Affairs, Biostatistics, Oncology Product, and Commercial functions.

Matching Summary

Match Score: 75

** Natera is seeking a Senior Director for Oncology Clinical Trial Operations in San Carlos, CA, to lead the strategic planning and execution of oncology clinical trials. The ideal candidate will have extensive experience in clinical research, particularly in oncology, and will be responsible for overseeing trial operations, managing CRO relationships, and ensuring compliance with regulatory standards. **

Skills & Requirements

Must-have

  • Oncology clinical trial execution
  • CRO selection and oversight
  • GCP compliance and inspection readiness
  • Clinical trial budget management
  • Cross-functional team leadership

Nice-to-have

  • Entrepreneurial company environment
  • Hands-on leadership approach
  • Adaptable to fast-paced environment

Key Requirements

  • Advanced degree preferred (MS, Pharm D, MD, or PhD)
  • >10 years clinical research experience
  • 5+ years managing clinical trials in a leading role
  • Significant global CRO leadership experience
  • Extensive oncology clinical trial program experience
  • Knowledge of FDA and/or EMEA Regulations, and GCPs

Work Rights

Not specified

Tailored Resume

Cover Letter