Global Clinical Trial Leader (Hybrid)

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