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Global Clinical Trial Leader (Hybrid)

Dawar Consulting, Inc.
Posted 14 days ago, valid for 9 days
Location

South San Francisco, CA, US

Salary

$103 per day

Contract type

Contract

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Sonic Summary

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  • Our client, a leader in life sciences and biotechnology, is seeking a Global Clinical Trial Leader in SSF, CA (Hybrid).
  • This long-term contract position offers a pay rate of $103 per hour on a W2 basis, with benefits including medical, paid sick leave, and 401K.
  • The role requires 8+ years of clinical study management experience, focusing on the execution of complex early-phase global clinical trials (Phase I/II).
  • Key responsibilities include providing operational leadership, managing CROs and vendors, and ensuring successful trial execution through collaboration with cross-functional teams.
  • Candidates should have a bachelor's degree in a scientific or healthcare discipline and possess strong knowledge of GCP/ICH and international regulatory requirements.

Our client, a worldleader in life sciences and biotechnology, is looking for aĀ ā€œGlobalClinical Trial Leaderā€ based in SSF, CA (Hybrid).

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Job Duration:Ā LongTerm ContractĀ (Possibility Of Extension)

Pay Rate : $103/hr onW2

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Company Benefits: Medical, Paid Sickleave, 401K

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The Global ClinicalTrial Leader (CTL) will support the execution and delivery of complexearly-phase global clinical trials (Phase I/II) for innovative new molecularentities. Working under the Sr. CTL, this role provides operational leadershipacross study start-up, conduct, and close-out while coordinatingcross-functional teams, CROs, and vendors.

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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.
  • Manage CROs/vendors, including performance, scope, deliverables, and assigned budgets.
  • Drive key 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.
  • Support a patient- and site-centric approach to clinical trial execution.
  • Act as an SME, mentor colleagues, and contribute to organizational change initiatives.

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RequiredQualifications:

  • Bachelorā€™s degree or equivalent; scientific/healthcare discipline preferred.
  • 8+ years of clinical study management experience preferred.
  • Hands-on experience managing delegated aspects of global Phase I/II clinical trials.
  • Strong CRO/vendor management experience.
  • Knowledge of GCP/ICH, international regulatory requirements, and end-to-end drug development.

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If interested, pleasesend us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com

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