Gilead Sciences, Inc. is hiring a Director, Regional Community Oncology Expert (RCOE) – West within US Medical Affairs (USMA) Oncology to support the Community Oncology strategy and lead the Community Cancer Collective (CCC) in the West region. You will be responsible for co-developing strategy, leading CCC efforts in your territory, and supporting cross-functional field matrix teams.
What You'll Do
- Support the development of strategies and implementation plans for education, research, and Medical Affairs insights/data generation within US Community Oncology practices.
- Prepare and present scientific data at internal meetings and external advisory boards.
- Co-create a Real-World Evidence (RWE) generation plan with key US Community Oncology practices and initiate key RWE studies for Trodelvy and other molecules.
- Provide medical and scientific leadership at key scientific meetings with US HCPs and patients, focusing on Community Oncology.
- Serve as an educational resource and trainer to Gilead colleagues on medical educational activities, grants, and studies.
- Collaborate with Medical Affairs Research (MAR), Global/Local Review Committees, and Clinical R&D as needed.
- Deliver timely, accurate, and fair-balanced clinical and scientific presentations to Community Oncology healthcare professionals.
- Participate in the editorial review of all relevant scientific content for strategic alignment and accuracy.
- Critically review global investigator-sponsored research (ISR), collaborative, Ph3b, and Ph4 study proposals from US Community Oncology practices.
- Review abstracts and manuscripts from collaborative and RWE studies from Community Oncology practices.
- Communicate Gilead’s commitment to scientific excellence through research and education in Community Oncology practices.
- Collaborate effectively and compliantly with colleagues in other functional areas within Gilead.
- Support the development, deployment, and appropriate use of field tools and resources for the CCC.
- Lead oncology medical assets through the Medical Review Committee (MRC) process.
- Serve as the specific point of contact for cross-functional field matrix teams within their territory to create a One Oncology approach.
- Serve as a CCC resource to the field matrix team and provide training at national and regional levels for medical and commercial colleagues.
- Lead CCC projects/studies autonomously, establishing relationships with internal and external contacts as needed.
- Select sites for participation in the CCC based on objective criteria.
- Identify and develop relationships with regional and national opinion leaders to support the CCC.
- Anticipate and resolve complex obstacles in the field in a compliant and collaborative manner.
- Maintain familiarity with complex scientific data and commit to continuing education.
- Work as a member of several teams, such as MSL, MKAL, Key Account Directors (KADs), and national accounts.
- Lead relationships with vendors and collaborators on the delivery of materials like the CCC Playbook, Newsletter, Dashboard, and MRC documents.
- Contribute to the development of Global and Local strategic plans and collaborate with other functional areas.
- Support CCC efforts and strategic planning for US-based Oncology Societies focused on community engagement.
- Adhere to all applicable pharmaceutical codes, OIG guidelines, and Gilead policies.
What We're Looking For
- Oncology experience is required.
- If no advanced medical/scientific/clinical degree: MA/MS or MBA with 10+ years OR BA/BS with 12+ years of experience in the pharmaceutical industry or healthcare setting.
- If no Medical Affairs industry experience: success in a similar role outside of Medical Affairs in the biotech/pharmaceutical industry is required.
- Strong business acumen; ability to translate scientific expertise to achieve company goals.
- Demonstrated ability to think strategically and translate strategy into an actionable work plan.
- Excellent written, verbal, interpersonal, relationship-building, negotiating, and communication skills.
- Capacity to develop and deliver high-quality presentations.
- Excellent project management and organizational skills to anticipate and prioritize workloads.
- Affinity for a collaborative, team-oriented environment; ability to network with internal and external stakeholders.
- 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 data.
- Experience in developing effective abstracts, manuscripts, posters, and slides and presenting at scientific meetings.
- Must be fully cognizant of, and adhere to, regulatory, legal, and compliance requirements for clinical trials and Medical Affairs activities.
- Demonstrated ability to work with a high level of autonomy and independence.
- Ability to travel up to 70% of the time and occasionally on short notice, mainly US travel including territory, national/regional meetings, and HQ.
Nice to Have
- Advanced medical, scientific or clinical degree (e.g., PhD, MD, PharmD, NP or PA) with 8+ years experience in the pharmaceutical industry or healthcare setting.
- Industry experience in Medical Affairs.
- Experience working with Community Oncology practices and/or organizations.
- Thorough knowledge of FDA regulations, ICH guidelines, and GCPs governing the conduct of clinical trials.
Team & Environment
This role reports to the Senior Director, Community Oncology Strategy and Head of the CCC within the USMA Oncology team and works with cross-functional field matrix teams.
Benefits & Compensation
- Compensation: $221,000.00 - $286,000.00
- Company-sponsored medical, dental, vision, and life insurance plans
- Paid time off
- Discretionary annual bonus
- Discretionary stock-based long-term incentives
Work Mode
This position is remote and covers the West Region territory.
Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences.
