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Global Clinical Trial Leader (Hybrid
Job in
South San Francisco, San Mateo County, California, 94083, USA
Listed on 2026-08-08
Listing for:
JobRx, Inc.
Full Time
position Listed on 2026-08-08
Job specializations:
-
Science
Clinical Research
Job Description & How to Apply Below
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.
- 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.
- Early development clinical trial experience.
- Global study execution and operational strategy experience.
Experience managing complex, multi-country clinical studies.
Some travel may be required.
ContactIf interested, please send us your updated resume to or
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