Director, Medical Affairs Oncology, Strategic Evidence – Collaborations

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $221k - $314.6k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Gilead Sciences

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

💰 $3.5M Post-IPO Debt - Gilead Sciences on 2024-11

Healthcare • 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

• Co-develop US Medical Affairs congress plans with the Congress Center of Excellence and US Medical Affairs strategy and field-based medical teams • Represent and consider the US healthcare environment with internal and external stakeholders across approved and pipeline oncology therapies • Establish and execute an overarching US evidence-generation strategy across tumor types • Collaborate with cooperative groups, NCI/CTEP, and other key organizations • Provide input into US and Global Medical Affairs Strategic Plans, including the Integrated Strategic Plan and Plans of Action • Develop strategies and implementation plans addressing education, research, medical affairs insights, and data-generation needs • Prepare presentation materials and present scientific data at internal meetings and external advisory boards • Support global and regional congress strategic planning and tactical execution • Lead or support US Medical Affairs strategic planning for US-based oncology societies • Provide medical and scientific leadership at key scientific meetings with US healthcare professionals and patients • Serve as an information resource to Gilead colleagues, including US Medical Science Liaisons, for medical education, grants, and investigator-sponsored or collaborative studies • Collaborate on Collaboration Research with Medical Affairs Research and Clinical R&D • Deliver timely, accurate, succinct, fair-balanced clinical and scientific presentations to healthcare professionals when needed • Participate in editorial review of scientific content for strategic alignment and accuracy • Support disease-specific publication strategy and review US collaboration research abstracts and manuscripts • Communicate Gilead’s commitment to scientific excellence through research and education • Collaborate compliantly with colleagues across Gilead • Perform other activities supporting US Medical Affairs strategy development and tactical execution

🎯 Requirements

• Advanced medical/scientific degree such as Ph.D., MD, or PharmD and 8+ years of Medical Affairs experience or similar experience outside biotech/pharmaceuticals; OR MA/MS and 10+ years of experience; OR BA/BS and 12+ years of experience • Minimum 8 years of experience under the lowest qualifying education alternative • Experience specific to oncology preferred • Ability to think strategically and translate strategy into an actionable work plan • Excellent written, verbal, interpersonal, relationship-building, negotiating, and communication skills • Excellent organizational skills for project planning across multiple activities and workload prioritization • Excellent teamwork skills • Attention to detail and ability to meet timelines in a fast-paced environment • Excellent analytical and problem-solving skills, including identifying complex issues and querying key findings from study data and publications • Experience developing abstracts, manuscripts, posters, and slides and presenting at scientific meetings • Thorough knowledge of FDA regulations, ICH guidelines, and GCPs governing clinical trials preferred • Must adhere to regulatory and legal Business Conduct requirements for clinical trials and Medical Affairs activities • Ability to work with a high level of autonomy and independence • Must be able to travel more than 50% of the time, including domestic and international travel

🏖️ Benefits

• Discretionary annual bonus eligibility • Discretionary stock-based long-term incentives eligibility may vary based on role • Paid time off • Company-sponsored medical insurance • Company-sponsored dental insurance • Company-sponsored vision insurance • Company-sponsored life insurance • Benefits package