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Global Clinical Trial Leader; Hybrid

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: Dawar Consulting, Inc.
Full Time position
Listed on 2026-09-12
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 210000 - 220000 USD Yearly USD 210000.00 220000.00 YEAR
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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