Associate Director, Field Medical Affairs – Cutaneous Oncology

This is a fully remote position, open to applicants in Kentucky, +4 more states.

📋 Description

• Participate in the sharing of scientific data and various medical and/or scientific information with Key Opinion Leaders (KOLs), Healthcare Professionals (HCPs), researchers, pharmacists, and decision-makers based on population health.

• Exhibit a comprehensive understanding of solid tumors, including cutaneous oncology and other relevant tumors within clinical development that align with strategic medical initiatives.

• Build, nurture, and sustain professional relationships with KOLs.

• Serve as the main clinical/scientific authority for HCPs concerning disease states and company offerings.

• Identify and maintain a roster of pertinent medical and therapeutic area experts and investigators, and create engagement strategies.

• Assist in generating evidence through company-sponsored clinical trials and investigator-led studies.

• Recognize and communicate medical insights.

• Detect research deficiencies and educational requirements to guide medical strategies.

• Address information inquiries and present or discuss scientific and clinical data with suitable audiences while adhering to compliance standards.

• Conduct disease management and provide therapeutic area education to practitioners, payers, and researchers.

• Attend medical conferences to gather and relay scientific, clinical, and competitive intelligence to internal stakeholders.

• Uphold company policies, procedures, principles, and financial controls with professionalism and integrity.

⛳️ Requirements

• A terminal scientific degree (MD, PharmD, PhD, DNP, or DVM) is mandatory.

• 8+ years of relevant experience, including at least 4 years as an Oncology Medical Science Liaison.

• Knowledge or experience within the Oncology therapeutic area is essential.

• Experience in cutaneous oncology is advantageous.

• Established connections with KOLs in thoracic malignancies and familiarity with institutions focused on Solid Tumor Malignancies is preferred.

• Experience with drug launches is highly desirable.

• Understanding of treatment guidelines, clinical research protocols, FDA regulations, pharmaceutical regulations/compliance practices, and OIG guidelines is important.

• Residency within the designated territory is required.

• A valid driver’s license and a clean driving record must be maintained.

• Willingness to travel approximately 50%, including air travel, overnight stays, and occasionally on weekends.

🏝️ Benefits

• Annual bonuses or alternative incentive plans.

• Equity awards.

• Pension or retirement benefits.

• 401(k) company matching contributions.

• Health and wellness initiatives.

• Access to fitness centers.

• Comprehensive medical, dental, vision, life, and disability insurance benefits.

• Paid time off.

• Family support benefits.

• Reasonable accommodations during the recruitment process as needed.