Job Details

Global Clinical Trial Leader (Hybrid)

  2026-06-10     Dawar Consulting     South San Francisco,CA  
Description:

Global Clinical Trial Leader

Our client, a world leader in biotechnology and life sciences, is looking for a Global Clinical Trial Leader based out of South San Francisco, CA (Hybrid). Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate: $90/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K

Support the execution and delivery of global Phase I and II clinical trials within Research and Early Development (RED). Partner with cross-functional teams, vendors, and stakeholders to ensure successful study execution, risk management, operational excellence, and compliance with GCP/ICH and regulatory requirements.

Key Responsibilities:

  • Provide operational leadership and guidance to global cross-functional Protocol Execution Teams (PETs) across study start-up, conduct, and close-out activities.
  • Drive delivery of key trial deliverables including vendor specifications, drug supply forecasting, monitoring plans, TMF, and CTMS documentation.
  • Collaborate with cross-functional stakeholders on study planning, protocol feasibility, site selection, and investigator meetings.
  • Manage CROs and vendors to ensure performance aligns with contracted scope, timelines, quality, and budget expectations.
  • Contribute to study budget planning and oversee assigned vendor budgets.
  • Identify operational risks, develop mitigation strategies, and proactively manage study timelines and issues.
  • Support process improvement initiatives and contribute to clinical operations best practices.
  • Mentor junior team members and serve as a subject matter expert for designated initiatives.

Qualifications:

  • Bachelor's degree required; scientific or healthcare-related discipline preferred.
  • 8+ years of clinical study management experience within the pharmaceutical, biotech, or CRO industry.
  • Experience supporting global Phase I and/or Phase II clinical trials.
  • Strong vendor and CRO management experience.
  • Working knowledge of GCP, ICH guidelines, international regulations, and the drug development process.
  • Preferred Experience:
    • Early development clinical trial experience.
    • Global study execution and operational strategy experience.
    • Experience managing complex, multi-country clinical studies.
  • Travel: Some travel may be required.

If interested, please send us your updated resume at hr@dawarconsulting.com / akansha@dawarconsulting.com


Apply for this Job

Please use the APPLY HERE link below to view additional details and application instructions.

Apply Here

Back to Search