Clinical Trials Manager, Early Phase Oncology (Remote)

Gilead Sciences, Inc.

Job Overview

Location

United States – Remote

Job Type

Full-time

Full Job Description

📋 Description

• Manage end-to-end operational delivery of early-phase oncology clinical trials, ensuring high-quality execution through cross-functional leadership and oversight of CROs and vendors.
• Coordinate and supervise all aspects of clinical study activities, including protocol development, informed consent forms, case report forms, monitoring plans, investigator brochures, and clinical study reports.
• Maintain accurate and timely study timelines to meet deliverables for in-house and hybrid model clinical trials.
• Contribute to the development of study budgets and participate in the selection of CROs and vendors through RFP processes.
• Coordinate review of clinical data listings and support preparation of interim and final clinical study reports.
• May contribute to the development of scientific abstracts, presentations, and manuscripts for internal and external communication.
• Ensure effectiveness and efficiency of site budget and contract processes.
• Train CROs, vendors, investigators, and study coordinators on study-specific requirements and regulatory expectations.
• Assist Clinical Program Manager in overall study management and prioritization of project activities within the functional area.
• Design and implement scientific communications within the company under supervision.
• Apply thorough knowledge of FDA and EMEA regulations, ICH guidelines, and GCPs governing clinical trial conduct.
• Interpret and clearly explain protocol requirements to internal teams and external partners.
• Prioritize and manage multiple competing tasks effectively in a fast-paced environment.
• Serve as a resource for clinical trials management expertise across the organization.
• Examine functional issues from an organizational perspective under general supervision.
• Participate in departmental and interdepartmental strategic initiatives with limited oversight.
• Support the development and implementation of standard operating procedures (SOPs).
• Travel is required as part of the role.
• Demonstrate excellent teamwork, communication, decision-making, and organizational skills.

🎯 Requirements

• Bachelor’s Degree and five years’ experience in a relevant scientific discipline OR Master’s Degree and three years’ experience in a relevant scientific discipline
• Prior CRO/Pharma experience REQUIRED
• Prior Oncology experience REQUIRED

🏖️ Benefits

• Salary range of $133,195.00 - $172,370.00
• Eligibility for discretionary annual bonus
• Eligibility for discretionary stock-based long-term incentives
• Comprehensive benefits package including medical, dental, vision, and life insurance
• Paid time off
• Access to company-sponsored wellbeing programs

Skills & Technologies

Remote

Degree Required

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Gilead Sciences, Inc.

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About Gilead Sciences, Inc.

Biopharmaceutical company discovering, developing and commercializing medicines in virology, oncology and inflammation. Founded in 1987, it focuses on antiviral therapies for HIV, hepatitis B and C, COVID-19, and investigational treatments for cancer and fibrotic diseases. Operations span research, manufacturing and global access programs.

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