
10,000+ employees
Founded 1987
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Gilead Sciences is a leading biopharmaceutical company that focuses on discovering, developing, and delivering innovative therapeutics for patients with life-threatening diseases. The company is highly recognized for its contributions in virology, particularly HIV and hepatitis, and is actively expanding its therapeutic reach into fields like oncology and inflammation. Gilead has a strong pipeline of medicines, with over 25 products available globally and 50 clinical programs. Known for its commitment to health equity, the company also actively funds HIV research and causes. Gilead's dedication to scientific innovation and health equity aims to tackle the world's most pressing health challenges, improving patient lives globally.
🕒 June 3
🇺🇸 United States – Remote
💵 $133.2k - $172.4k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
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10,000+ employees
Founded 1987
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Gilead Sciences is a leading biopharmaceutical company that focuses on discovering, developing, and delivering innovative therapeutics for patients with life-threatening diseases. The company is highly recognized for its contributions in virology, particularly HIV and hepatitis, and is actively expanding its therapeutic reach into fields like oncology and inflammation. Gilead has a strong pipeline of medicines, with over 25 products available globally and 50 clinical programs. Known for its commitment to health equity, the company also actively funds HIV research and causes. Gilead's dedication to scientific innovation and health equity aims to tackle the world's most pressing health challenges, improving patient lives globally.
• 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 • Coordinates with internal teams and external partners (including CROs and vendors) • Maintains study timelines, including documentation and communications • Provides oversight of study sites/region and reviews routine regulatory documents
• 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 • Strong project management skills • Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs
• Health insurance • Dental insurance • Vision insurance • Life insurance • Paid time off • Discretionary annual bonus • Discretionary stock-based long-term incentives
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