Director, Strategic Evidence and Collaborations

🔥 0 minutes ago

🏄 California – Remote

🏄 California – Remote

💵 $243.1k - $314.6k / year

⏰ Full Time

🔴 Lead

👔 Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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 strategy for congress plans with the Congress Center of Excellence, USMA Strategy, and Field Based Medical Teams • Represent and consider the US healthcare environment with internal and external stakeholders across approved and pipeline cancer therapies • Establish and execute an overarching US evidence-generation strategy across various 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 • Demonstrate subject matter expertise in the ADC portfolio, Gilead clinical trials, clinical use, and competitive products • Contribute to Community Cancer Collective Team work • 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, regional, and US 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 patient presence • Serve as an information resource for Gilead colleagues, including Medical Science Liaisons, on medical education, grants, and investigator-sponsored/collaborative studies • Collaborate on Collaboration Research with the Medical Affairs Research Team and Clinical R&D • Occasionally deliver timely, accurate, succinct, and fair-balanced clinical and scientific presentations to healthcare professionals in compliance with promotional and regulatory requirements • Participate in editorial review of scientific content for strategic alignment and accuracy • Support disease-specific publication strategy • Critically review global collaboration research, Phase 3b, and Phase 4 study proposals generated in the US • Review abstracts and manuscripts from US collaboration research • 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 (Ph.D., MD, or Pharm D) and 8+ years of experience in Medical Affairs or success in a similar role outside of the biotech/pharmaceutical industry, OR MA/MS and 10+ years of experience, OR BA/BS and 12+ years of experience • Experience specific to oncology • Demonstrated 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 • Ability to identify and understand complex issues and query key findings from study data and publications • Experience developing abstracts, manuscripts, posters, and slides and presenting at scientific meetings • Must adhere to regulatory and legal Business Conduct requirements for clinical trials and Medical Affairs activities • Thorough knowledge of FDA regulations, ICH guidelines, and GCPs governing clinical trials is preferred • 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 • Equal employment opportunity and reasonable accommodation support