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Global Clinical Trial Leader; Hybrid
Job in
South San Francisco, San Mateo County, California, 94083, USA
Listed on 2026-09-12
Listing for:
Dawar Consulting, Inc.
Full Time
position Listed on 2026-09-12
Job specializations:
-
Science
Clinical Research
Job Description & How to Apply Below
Global Clinical Trial Leader (Hybrid)
South San Francisco, United States | Posted on 09/08/2026
Our client, a world leader in life sciences and biotechnology, is looking for a“Global Clinical Trial Leader” based in SSF, CA (Hybrid).
Job Duration:
Long Term Contract(Possibility Of Extension)
Pay Rate : $103/hr onW2
Company Benefits:- Medical
- Paid Sickleave
- 401K
The Global Clinical Trial Leader (CTL) will support the execution and delivery of complex early-phase global clinical trials (Phase I/II) for innovative new molecular entities. Working under the Sr. CTL, this role provides operational leadership across study start-up, conduct, and close-out while coordinating cross-functional teams, CROs, and vendors.
Key Responsibilities:
- Provide operational leadership to global Protocol Execution Teams (PETs) throughout the trial lifecycle.
- Support study planning, site/country feasibility, protocol execution, timelines,and risk mitigation.
- ManageCROs/vendors, including performance, scope, deliverables, and assigned budgets.
- Drivekey study documentation, including TMF, CTMS, monitoring plans, drug supply forecasting, and vendor specifications.
- Collaborate with cross-functional teams and investigators to ensure successful trial execution.
- Identify operational risks, bottlenecks, and issues and develop practical solutions.
- Contribute to process improvements and operational best practices across gRED/Roche.
- Supporta patient- and site-centric approach to clinical trial execution.
- Actas an SME, mentor colleagues, and contribute to organizational change initiatives.
Required Qualifications:
- 8+years of clinical study management experience preferred.
- Hands-on experience managing delegated aspects of global Phase I/II clinical trials.
- Knowledge of GCP/ICH, international regulatory requirements, and end-to-end drug development.
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