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Global Clinical Trial Leader (Hybrid

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: JobRx, Inc.
Full Time position
Listed on 2026-08-08
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 90000 USD Yearly USD 90000.00 YEAR
Job Description & How to Apply Below
Position: Global Clinical Trial Leader (Hybrid)

Job Description

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, drugsupply forecasting, monitoring plans, TMF, and CTMS documentation.
  • Collaborate with cross-functional stakeholders on study planning, protocolfeasibility, site selection, and investigator meetings.
  • ManageCROs 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 managestudy 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 designatedinitiatives.
Qualifications
  • Bachelor'sdegree 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.
  • Strongvendor 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.

Contact

If interested, please send us your updated resume to  or

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