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Dawar Consulting, Inc.

Dawar Consulting, Inc.

Global Clinical Trial Leader (Hybrid)

South San Francisco, USOfisteSözleşmeliTam zamanlı

9 Eyl 2026 tarihinde yayınlandı

Bu iş EN dilinde yayınlanmıştır

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 on W2


Company Benefits: Medical, Paid Sick leave, 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.
  • 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.


Required Qualifications:

  • Bachelor’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.


If interested, please send us your updated resume at

hr@dawarconsulting.com/akansha@dawarconsulting.com




Rol özeti

İş türü

Tam zamanlı

Gerekli beceriler

Clinical Study ManagementGlobal Phase I/II Trial ExecutionProtocol Development & ExecutionCRO and Vendor ManagementTrial Master File (TMF) ManagementClinical Trial Management System (CTMS) AdministrationDrug Supply Forecasting & LogisticsMonitoring Plan DevelopmentGCP/ICH and International Regulatory RequirementsRisk Management and Issue ResolutionCross-functional Stakeholder CollaborationTeam Leadership, Mentoring & Subject Matter ExpertiseSite and Country Feasibility AssessmentStudy Budget Management (assigned budgets)

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