Regional Director – Medical Affairs, GYN Malignancies

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2 days ago

🔔 Pennsylvania – Remote

Although this job is listed in Pennsylvania, this company may be open to hiring remote in other states.

💵 $206.2k - $324.6k / year

⏰ Full Time

🔴 Lead

👔 Director

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MSD

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Biotechnology • Pharmaceuticals • Healthcare Insurance

MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.

10,000+ employees

Founded 1891

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Develops and executes US Medical Affairs strategy for Gynecologic malignancies • Drives creation and facilitation of training materials for the Oncology Medical Affairs team through the appropriate review systems and serves as the medical approver of these materials • Designs, updates and gives training both internally and externally in collaboration with the global scientific training and content teams • Coordinates, presents at and leads Advisory Boards and other meetings with US Scientific Leaders • Engages in scientific exchange with Scientific Leaders to obtain input on disease landscape, current data, and evidence gaps • Helps with planning of various aligned activities around major oncology congresses. • Supports commercial group for Launch Preparation and Post-launch activities • Serves as a member on the Value Evidence sub-team for Gynecologic Cancer internal stakeholders’ expectations with timely updates • Interacts with internal stakeholders for needs assessment and planning. • Leads strategy and interactions with Patient Advocacy Groups • Tracks guidelines and regulatory landscape in the US region • Review of Investigator Initiated Studies • Collaborates and leads interaction with our external collaboration partners with whom we co-develop oncology products.

🎯 Requirements

• Advanced degree: MD, PhD, PharmD • Minimum five years of experience at a pharmaceutical or biotechnology company in Oncology, working in medical affairs leading cross functional matrix teams. • Strong leadership skills and ability to effectively collaborate with and influence partners within and across divisions. • Proven ability to collaborate with others and to resolve conflicts. • Outstanding verbal and written communications skills.

🏖️ Benefits

• medical, dental, vision healthcare and other insurance benefits (for employee and family) • retirement benefits, including 401(k) • paid holidays • vacation • compassionate and sick days