Gilead Sciences
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
💰 $3.5M Post-IPO Debt - Gilead Sciences on 2024-11
Biotechnology • Pharmaceuticals
Gilead Sciences is a global biopharmaceutical company focused on researching, developing, and commercializing medicines primarily in virology, oncology, and inflammation. The company advances transformative therapies, runs extensive clinical programs and research collaborations, and supports access, global health, and community funding initiatives. Gilead also emphasizes corporate responsibility, sustainability, and inclusion while maintaining a broad pipeline of therapies and patient access programs.
Clinical Trials Manager – Late Phase Oncology
🕒 June 4
🇺🇸 United States – Remote
💵 $133.2k - $172.4k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
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Gilead Sciences
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
💰 $3.5M Post-IPO Debt - Gilead Sciences on 2024-11
Biotechnology • Pharmaceuticals
Gilead Sciences is a global biopharmaceutical company focused on researching, developing, and commercializing medicines primarily in virology, oncology, and inflammation. The company advances transformative therapies, runs extensive clinical programs and research collaborations, and supports access, global health, and community funding initiatives. Gilead also emphasizes corporate responsibility, sustainability, and inclusion while maintaining a broad pipeline of therapies and patient access programs.
📋 Description
• Drive end-to-end operational delivery of Phase II and III oncology trials • Ensure high-quality execution through strong cross-functional leadership and CRO/vendor oversight • Coordinate with internal teams and external partners (including CROs and vendors) • Implement solutions, and maintain study timelines to meet study deliverables • Provide oversight of study sites/region and review routine regulatory documents • Train CROs, vendors, investigators, and study coordinators on study requirements
🎯 Requirements
• 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 is desirable
🏖️ Benefits
• Discretionary annual bonus • Discretionary stock-based long-term incentives (eligibility may vary based on role) • Paid time off • Company-sponsored medical, dental, vision, and life insurance plans
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