Director, Regional Community Oncology Expert – East

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🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $221k - $286k / year

⏰ Full Time

🔴 Lead

👫 Community Manager

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Gilead Sciences

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Co-develop the Community Oncology strategy and lead Community Cancer Collective efforts in the assigned territory • Support cross-functional field matrix teams and represent Community Oncology with internal and external stakeholders • Develop strategies and implementation plans addressing education, research, Medical Affairs insights, and data-generation needs • Prepare and present scientific data at internal meetings and external advisory boards • Co-create real-world evidence generation plans and initiate studies supporting Trodelvy in breast cancer and potentially other molecules, indications, and disease areas • Provide medical and scientific leadership at scientific meetings and engage US healthcare professionals and patients • Train Gilead colleagues, including MSLs and MKALs, on medical education, grants, and investigator-sponsored or collaborative studies • Lead compliant communication of fair-balanced clinical and scientific presentations to Community Oncology healthcare professionals • Participate in editorial review of scientific content for strategic alignment and accuracy • Critically review investigator-sponsored, collaborative, Phase 3b, and Phase 4 study proposals • Review abstracts and manuscripts resulting from collaborative and real-world evidence studies • Develop, deploy, and appropriately use field tools and resources for the Community Cancer Collective • Lead oncology medical assets through the Medical Review Committee process • Serve as the territory point of contact for cross-functional field matrix teams and support a One Oncology approach • Lead Community Cancer Collective projects and studies, selecting participating sites and developing relationships with opinion leaders and institutional leaders • Resolve complex field obstacles compliantly and collaboratively • Lead vendor and collaborator relationships for the CCC Playbook, newsletters, dashboard, and medical communications • Support strategic planning for US-based oncology societies focused on community engagement • Adhere to pharmaceutical codes, OIG guidelines, Gilead policies, and applicable regulatory, legal, and compliance requirements • As a people leader, create inclusion, develop talent, and empower teams

🎯 Requirements

• Bachelor's Degree and 12 years' experience OR Master's Degree and 10 years' experience OR PhD/PharmD and 8 years' experience • Advanced medical, scientific, or clinical degree such as PhD, MD, PharmD, NP, or PA preferred • Industry experience in Medical Affairs • Oncology experience preferred • Experience working with Community Oncology practices and/or organizations preferred • Strong business acumen and ability to translate scientific expertise into company goals • Ability to think strategically and translate strategy into an actionable work plan • Excellent written, verbal, interpersonal, relationship-building, negotiating, and communication skills • Ability to develop and deliver high-quality presentations • Excellent project management and organizational skills • Ability to collaborate and partner with internal and external stakeholders, including C-suite and healthcare professionals • Attention to detail and ability to meet timelines in a fast-paced environment • Excellent analytical and problem-solving skills, including interpreting study data and publications • Experience developing abstracts, manuscripts, posters, and slides and presenting at scientific meetings • Must adhere to regulatory, legal, and compliance requirements for clinical trials and Medical Affairs activities • Thorough knowledge of FDA regulations, ICH guidelines, and GCPs governing clinical trials preferred • Ability to work with a high level of autonomy and independence • Ability to travel up to 70% of the time, occasionally on short notice, mainly within the United States

🏖️ Benefits

• Discretionary annual bonus eligibility • Discretionary stock-based long-term incentives eligibility • Paid time off • Company-sponsored medical insurance • Company-sponsored dental insurance • Company-sponsored vision insurance • Company-sponsored life insurance