Clinical Program Manager, Medical Affairs Research Operations

Gilead Sciences

Foster City, CA, US
Base: $182,070.00 - $235,620.00; bonus/equity: dis...
Hybrid (3 days in office)
Bachelor's or master's degree with relevant experience
8+ years of experience in medical affairs research operations
Oversight of investigator initiated research (iir) and collaborative studies
Gilead Sciences is seeking a Clinical Program Manager for its Medical Affairs Research Operations to oversee Investigator Initiated Research and Collaborative programs. This hybrid role requires strong leadership and communication skills, along with a comprehensive understanding of Medical Affairs and clinical operations

Job Summary

  • The role involves providing oversight of Investigator Initiated Research and Collaborative programs across Gilead's therapeutic areas while ensuring regulatory compliance.
  • Candidates will lead departmental strategic initiatives, manage study managers, and act as an escalation point for issue resolution within a hybrid office-based setting.
  • Gilead offers a competitive salary range of $182,070.00 - $235,620.00 along with discretionary bonuses, stock incentives, and comprehensive benefits including medical and dental insurance.

Matching Summary

Match Score: 85

Gilead Sciences is seeking a Clinical Program Manager for its Medical Affairs Research Operations to oversee Investigator Initiated Research and Collaborative programs. This hybrid role requires strong leadership and communication skills, along with a comprehensive understanding of Medical Affairs and clinical operations.

Salary

Base: $182,070.00 - $235,620.00; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives eligible; Benefits: Company-sponsored medical, dental, vision, life insurance, and paid time off

Skills & Requirements

Must-have

  • Bachelor's or Master's degree with relevant experience
  • 8+ years of experience in medical affairs research operations
  • Oversight of Investigator Initiated Research (IIR) and Collaborative studies
  • Strong knowledge of FDA/EMA regulations and ICH guidelines
  • Experience leading staff and mentoring junior employees

Nice-to-have

  • Prior supervisory or leadership experience preferred
  • Experience with Phase IV and non-interventional studies
  • Global or large affiliate experience in medical affairs
  • Ability to work independently in a fast-paced environment
  • Strong interpersonal and influence skills

Key Requirements

  • Bachelor's Degree + 6 Years Experience OR Masters' + 4 Years Experience
  • Preferred: 8+ years experience with RN or BS/BA in scientific discipline
  • Must have comprehensive understanding of FDA/EMA regulations and GCP
  • Required: Prior supervisory/leadership experience managing staff

Work Rights

Not specified

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