Remotery

Director, Regional Community Oncology Expert – East

Posted 20 hours ago

This is a fully remote position, open to applicants in United States.

📋 Description

• Collaborate in the development of the Community Oncology strategy while spearheading Community Cancer Collective initiatives within the designated territory.

• Assist cross-functional field matrix teams and represent Community Oncology to both internal and external stakeholders.

• Formulate strategies and implementation plans that address education, research, Medical Affairs insights, and data-generation requirements.

• Prepare and deliver scientific presentations at internal gatherings and external advisory boards.

• Co-create plans for real-world evidence generation and initiate studies that support Trodelvy in breast cancer as well as potentially other molecules, indications, and disease areas.

• Provide medical and scientific leadership at scientific conferences, engaging with US healthcare professionals and patients.

• Educate Gilead colleagues, including MSLs and MKALs, on medical education, grants, and investigator-sponsored or collaborative studies.

• Ensure compliant communication of fair-balanced clinical and scientific presentations to Community Oncology healthcare professionals.

• Participate in the editorial review of scientific content to ensure strategic alignment and accuracy.

• Conduct thorough reviews of investigator-sponsored, collaborative, Phase 3b, and Phase 4 study proposals.

• Review abstracts and manuscripts generated from collaborative and real-world evidence studies.

• Develop, implement, and effectively utilize field tools and resources for the Community Cancer Collective.

• Guide oncology medical assets through the Medical Review Committee process.

• Act as the territory point of contact for cross-functional field matrix teams and support a unified One Oncology approach.

• Oversee Community Cancer Collective projects and studies, selecting participating sites and fostering relationships with opinion leaders and institutional leaders.

• Address complex field challenges in a compliant and collaborative manner.

• Lead relationships with vendors and collaborators for the CCC Playbook, newsletters, dashboard, and medical communications.

• Assist in strategic planning for US-based oncology societies with a focus on community engagement.

• Comply with pharmaceutical codes, OIG guidelines, Gilead policies, and relevant regulatory, legal, and compliance obligations.

• As a leader, foster inclusion, develop talent, and empower teams.


⛳️ Requirements

• Bachelor's Degree and 12 years of experience OR Master's Degree and 10 years of experience OR PhD/PharmD and 8 years of experience.

• Preferred advanced medical, scientific, or clinical degree such as PhD, MD, PharmD, NP, or PA.

• Experience in the Medical Affairs sector is essential.

• Oncology experience is preferred.

• Experience working with Community Oncology practices and/or organizations is preferred.

• Strong business acumen and the capability to translate scientific expertise into organizational objectives.

• Strategic thinking ability to convert strategy into actionable work plans.

• Exceptional written, verbal, interpersonal, relationship-building, negotiation, and communication skills.

• Proven ability to develop and deliver high-quality presentations.

• Strong project management and organizational abilities.

• Capacity to collaborate and partner with internal and external stakeholders, including C-suite executives and healthcare professionals.

• Keen attention to detail and the ability to meet deadlines in a dynamic environment.

• Excellent analytical and problem-solving skills, including the ability to interpret study data and publications.

• Experience in developing abstracts, manuscripts, posters, and slides, and presenting at scientific meetings.

• Must comply with regulatory, legal, and compliance standards for clinical trials and Medical Affairs activities.

• Comprehensive knowledge of FDA regulations, ICH guidelines, and GCPs governing clinical trials is preferred.

• Ability to work autonomously and independently.

• Willingness to travel up to 70% of the time, occasionally on short notice, primarily within the United States.


🏝️ Benefits

• Eligibility for discretionary annual bonus.

• Eligibility for 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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