Clinical Trials Manager

Gilead Sciences

. Drive end-to-end operational delivery of Phase II and III oncology trials .

Posted 9/21/2026full-timeUnited StatesMid-LevelSenior💰 $133,195 - $172,370 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing Phase II and III oncology trials, including oversight of clinical study operations, regulatory compliance, and budget management. Proficient in coordinating with CROs and vendors while ensuring effective communication and documentation throughout the study lifecycle.

Highest-signal resume keywords

Oncology ExperienceCRO ManagementClinical Trial OversightFDA Regulations KnowledgeGCP Compliance

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Study Protocol DevelopmentBudget ManagementData Discrepancy ResolutionSOP DevelopmentClinical Study Report Preparation

Soft Skills

TeamworkCommunicationDecision-MakingOrganizational Skills

Industry Keywords

Clinical TrialsPharmaBiotechEMEA RegulationsICH Guidelines

About the role

Key responsibilities & impact

Drive end-to-end operational delivery of Phase II and III oncology trials
Coordinate and supervise all aspects of clinical studies
Assist the Clinical Program Manager in overall study management
Provide input into study protocols, investigator brochures, case report forms, informed consents, final study reports, study plans, and presentations
Maintain study timelines, documentation, and communications
Contribute to study budgets, RFPs, and CRO/vendor selection
Manage CROs, vendors, or functional service providers as needed
Provide operational contact and oversight for site evaluation, initiation, close-out, and monitoring visits
Oversee study sites/regions and review regulatory documents for compliance
Ensure effectiveness of site budget and contract processes
Train CROs, vendors, investigators, and study coordinators on study requirements as needed
Coordinate data listing reviews and preparation of interim/final clinical study reports and appendices
Resolve data discrepancies
Develop tools and processes to optimize project efficiency and effectiveness
Serve as a resource for clinical trials management expertise

Requirements

What you’ll need

Prior Oncology experience required
Prior CRO/Pharma/Biotech experience required
5+ years with BS/BA in a relevant scientific discipline
3+ years with MS/MA in a relevant scientific discipline
Travel is required
Excellent teamwork, communication, decision-making and organizational skills
Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable
Ability to understand, interpret, and explain protocol requirements
Ability to prioritize multiple tasks
General functional expertise to support SOP development and implementation

Benefits

Comp & perks

Discretionary annual bonus eligibility
Discretionary stock-based long-term incentives eligibility
Paid time off
Company-sponsored medical insurance
Company-sponsored dental insurance
Company-sponsored vision insurance
Company-sponsored life insurance
Reasonable accommodation during the job application process