Global Clinical Trial Leader (Hybrid)

Dawar Consulting, Inc.; South San Francisco (CA); Hybrid; USD 210,000 - 220,000; Full time

Benefits offered by this job

Medical

Paid Sickleave

401K

Job summary

Dawar Consulting, Inc. in South San Francisco, CA is seeking a Global Clinical Trial Leader for a long-term, hybrid role to lead global Phase I/II trials and coordinate cross-functional teams, CROs and vendors to deliver study milestones.

The candidate will provide operational leadership for protocol execution, feasibility, timelines, TMF/CTMS, drug supply forecasting, risk mitigation, and pursue process improvements in collaboration with gRED/Roche teams.

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.

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.

Job description

Global Clinical Trial Leader (Hybrid)

South San Francisco, United States | Posted on 09/08/2026

Our client, a worldleader in life sciences and biotechnology, is looking for a“GlobalClinical Trial Leader” based in SSF, CA (Hybrid).

Job Duration:LongTerm Contract(Possibility Of Extension)

Pay Rate : $103/hr onW2

Company Benefits:

• Medical
• Paid Sickleave
• 401K

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.

Key Responsibilities:

• Provideoperational leadership to global Protocol Execution Teams (PETs)throughout the trial lifecycle.


• Supportstudy planning, site/country feasibility, protocol execution, timelines,and risk mitigation.


• ManageCROs/vendors, including performance, scope, deliverables, and assignedbudgets.


• Drivekey study documentation, including TMF, CTMS, monitoring plans, drugsupply forecasting, and vendor specifications.


• Collaboratewith cross-functional teams and investigators to ensure successful trialexecution.


• Identifyoperational risks, bottlenecks, and issues and develop practicalsolutions.


• Contributeto 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 changeinitiatives.

RequiredQualifications:

• 8+years of clinical study management experience preferred.


• Hands-onexperience managing delegated aspects of global Phase I/II clinicaltrials.


• Knowledgeof GCP/ICH, international regulatory requirements, and end-to-end drugdevelopment.