Clinical Trials Manager – Late Phase Oncology

Gilead Sciences

Clinical Trials Manager managing operational delivery of Phase II and III oncology trials. Ensures high-quality execution and alignment across stakeholders at Gilead.

Posted 7/28/2026full-timeFoster City • California, New Jersey • 🇺🇸 United StatesMid-LevelSenior💰 $133,195 - $172,370 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing Phase II and III oncology trials, ensuring compliance with FDA and EMEA regulations, and applying strong project management skills to maintain study timelines and deliverables. Proven ability to lead cross-functional teams and coordinate with CROs and vendors to achieve study objectives.

Highest-signal resume keywords

Oncology ExperienceCRO OversightProject ManagementRegulatory ExpertiseClinical Trial Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study ManagementRisk IdentificationBudget DevelopmentRegulatory Document ReviewTimeline Maintenance

Soft Skills

TeamworkCommunicationDecision-MakingOrganizational Skills

Industry Keywords

FDA RegulationsEMEA RegulationsICH GuidelinesGCPsCROPharmaBiotech

About the role

Key responsibilities & impact

Drives end-to-end operational delivery of Phase II and III oncology trials
Ensures high-quality execution through strong cross-functional leadership and CRO/vendor oversight
Serves as a key contributor for study execution and study management
Coordinates with internal teams and external partners (including CROs and vendors) to ensure alignment across all stakeholders to achieve study objectives
Applies strong project management, clinical, and regulatory expertise to proactively identify risks, implement solutions, and maintain study timelines to meet study deliverables
Assists Clinical Program Manager in the overall study management
Maintains study timelines, including documentation and communications
Contributes to development of study budget
Provides oversight of study sites/region and review routine regulatory documents

Requirements

What you’ll need

5+ Years with BS/BA in a relevant scientific discipline
3+ Years with MS/MA in a relevant scientific discipline
Prior Oncology experience
Prior CRO/Pharma/Biotech experience
Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials
Excellent teamwork, communication, decision-making and organizational skills.

Benefits

Comp & perks

company-sponsored medical, dental, vision, and life insurance plans
paid time off
discretionary annual bonus
discretionary stock-based long-term incentives