
Field Medical Director, Solid Tumors
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in Alabama, +3 more states.
• Assist in the development of BeOne Medicines’ pre-clinical and clinical pipeline.
• Facilitate external collaborations and research initiatives with healthcare professionals and academic institutions.
• Promote internal collaboration throughout the organization.
• Create regional strategies for compliant engagement with opinion leaders, research partners, and key organizations.
• Offer pre-launch and post-launch Medical Affairs support for solid tumor pipeline products, with a focus on breast and lung cancers.
• Work collaboratively with medical affairs, clinical development, program management, clinical operations, legal, compliance, new product planning, safety/pharmacovigilance, molecular diagnostics, marketing, sales, and translational research teams.
• Formulate territory plans alongside cross-functional teams to educate healthcare professionals and enhance patient outcomes.
• Build and sustain scientifically credible peer-to-peer relationships with opinion leaders and healthcare providers.
• Manage and oversee strategic partnerships with scientific and clinical experts and organizations.
• Support major and regional congresses by engaging with thought leaders.
• Deliver balanced and accurate information to formulary decision-makers and P&T committee members.
• Identify and evaluate potential investigators and recommend sites for company-sponsored clinical trials.
• Coordinate the submission and review of investigator-sponsored research proposals.
• Assist in organizing regional medical meetings, advisory boards, consultant meetings, and investigator meetings.
• Act as an internal resource for clinical and scientific information.
• Provide insights on emerging clinical and scientific trends.
• Conduct research in therapeutic areas and analyze competitors.
• Foster relationships with internal experts.
• Identify opportunities for process improvements.
• Develop, monitor, execute, and report on goals and objectives.
• Aid in the planning and management of the Medical Affairs budget.
• Ensure adherence to compliant business practices.
• Experience in clinical oncology focusing on solid tumors; exceptional transferable experience in other therapeutic areas may be considered.
• Established relationships with relevant healthcare professionals in the region.
• Excellent written and verbal communication, interpersonal, organizational, and cross-functional collaboration abilities.
• Willingness to work with colleagues in a global environment.
• Willingness to travel for work approximately 60–70% of the time.
• MD, PharmD, PhD, or DO in a clinical and/or scientific field, with a minimum of 5 years’ clinical experience and/or success in other biotech/pharmaceutical companies; OR NP, PA, or Master’s Degree in a clinical and/or scientific field, with at least 6 years’ clinical experience and/or success in other biotech/pharmaceutical companies.
• Strong understanding of disease states, differential algorithms for treatment decisions, and relevant disease state experience.
• In-depth knowledge of the healthcare delivery system, managed care, regional medical care, and the pharmaceutical industry.
• Ability to identify unmet medical, educational, and research requirements.
• Capability to interpret scientific data and translate findings into educational and research needs.
• Familiarity with research study design, execution, and strategic implications.
• Proficiency in designing and/or leading training initiatives and best practices.
• Strong project management and leadership skills.
• Effective time management and organizational abilities.
• Annual bonus plan for Non-Commercial roles.
• Incentive compensation plan for Commercial roles.
• Discretionary equity awards.
• Employee Stock Purchase Plan.
• Medical insurance.
• Dental insurance.
• Vision insurance.
• 401(k) plan.
• FSA/HSA options.
• Life Insurance.
• Paid Time Off.
• Wellness programs.
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