Director, Regional Community Oncology Expert – East

Job not on LinkedIn

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $221k - $286k / year

⏰ Full Time

🔴 Lead

👫 Community Manager

🦅 H1B Visa Sponsor

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Logo of Gilead Sciences

Gilead Sciences

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 the Community Oncology strategy and implementation plans with the CCC Lead • Lead Community Cancer Collective efforts within the eastern United States territory • Support cross-functional field matrix teams and represent Community Oncology with internal and external stakeholders • Prepare presentation materials 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 other potential 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/collaborative studies • Deliver compliant, fair-balanced clinical and scientific communications to Community Oncology healthcare professionals • Participate in editorial review of scientific content • Review investigator-sponsored research, collaborative, Phase 3b, and Phase 4 study proposals, abstracts, and manuscripts • Develop and deploy field tools and resources for the Community Cancer Collective • Lead oncology medical assets through the Medical Review Committee process • Serve as the point of contact and CCC resource for cross-functional field matrix teams • Lead CCC projects and studies, select participating sites, and develop relationships with opinion leaders, institutional leaders, researchers, and providers • Lead vendor and collaborator relationships for CCC materials 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 and compliance requirements • Create inclusion, develop talent, and empower teams as a People Leader

🎯 Requirements

• Bachelor's Degree and 12 years' experience OR Master's Degree and 10 years' experience OR PhD/PharmD and 8 years' experience • Industry experience in Medical Affairs • Oncology experience and experience working with Community Oncology practices and/or organizations preferred • Advanced medical, scientific, or clinical degree preferred • Strong business acumen and ability to translate scientific expertise into company goals • Ability to think strategically and translate strategy into actionable work plans • 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 • Experience developing abstracts, manuscripts, posters, and slides and presenting at scientific meetings • 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, mainly within the US, including the territory, national and regional meetings, and headquarters • Must adhere to regulatory, legal, and compliance requirements for clinical trials and Medical Affairs activities

🏖️ Benefits

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

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