
10,000+ employees
Founded 1987
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
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.
🕒 May 1
🏄 California, New Jersey – Remote
💵 $261.4k - $338.3k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
👻 Ghost score 35%
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10,000+ employees
Founded 1987
🏥 Healthcare
💼 Consulting
🧬 Biotechnology
Healthcare • Consulting • Biotechnology
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.
• Provide clinical oversight and medical monitoring for one or more clinical trials in neurology and/or autoimmune disease • Contribute to the design and implementation of clinical studies, including early-phase and proof-of-concept trials • Draft and/or review protocols, protocol amendments, investigator brochures, clinical study reports, informed consent forms, safety narratives, and other clinical trial documents • Participate in investigator meetings, site engagement activities, and selected site initiation activities with clinical trial investigators • Support execution of clinical development plans by identifying study risks, proposing mitigations, and helping track milestones, deliverables, and budget-conscious study decisions
• MD or DO required • Approximately 2 to 5 years of clinical, scientific, and/or drug development experience in biopharma, academia, healthcare, or related settings • Working knowledge of clinical trial design, protocol development, safety review, and Good Clinical Practice • Ability to function effectively in a matrixed, cross-functional team environment
• Company-sponsored medical, dental, vision, and life insurance plans • Discretionary annual bonus • Discretionary stock-based long-term incentives (eligibility may vary based on role) • Paid time off
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