Director, Global Medical Affairs Strategy and Development

2 months ago

Plainsboro, New Jersey, United States Genmab Full time
Job Description

At Genmab, we're committed to building extraordinary futures together, by developing innovative antibody products and pioneering therapies that change the lives of patients and the future of cancer treatment and serious diseases.

We're seeking a highly skilled and experienced Director, Global Medical Affairs Strategy and Development to join our team. As a key member of our Medical Affairs Strategy Team, you will be responsible for developing and executing the global medical affairs strategic and tactical plans for our assets.

Key Responsibilities:

  • Develop and Execute Global Medical Affairs Strategy: Lead the development and execution of the global medical affairs strategic and tactical plans for our assets, in collaboration with cross-functional teams.
  • Lead Medical Planning: Lead annual medical planning for our assets, working closely with extended medical affairs functions to inform and implement overall medical strategy.
  • Engagement Strategy: Lead and execute on engagement strategy with thought leaders, patient advocacy groups, professional societies, and institutions.
  • Early Access Program and Investigator-Initiated Trials: Lead the planning and execution of Early Access Program and investigator-initiated trials, within appropriate standards for compliance, quality, timeliness, and budget.
  • Life Cycle Management: Contribute to the life cycle management of our assets, driving collaboration with cross-functional teams to provide support, medical review, and medical expertise advice.
  • Clinical Trial Activities: Collaborate with medical and clinical operations departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions.
  • Publication Planning: Contribute to effective publication planning to ensure consistent and meaningful scientific communication.
  • Regulatory Documents: Contribute to the development and review of regulatory documents for regulatory submissions.
  • Medical Review Committees: Serve as a medical reviewer and expert on promotional and medical review committees.

Requirements:

  • Scientific or Medical Degree: A scientific or medical degree (Pharm D, PhD, MD) is required.
  • Expertise in Solid Tumors: Expertise in the clinical landscape of solid tumors is required, with knowledge of gynecological cancers preferred.
  • Medical Affairs or Clinical Development Background: 7+ years of medical affairs or clinical development background in oncology is required.
  • Biotech/Pharmaceutical Industry Experience: Biotech/pharmaceutical industry experience, with a strong understanding of solid tumor drug development and medical affairs functions, is required.
  • Leadership and Collaboration Skills: Ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate across partnerships is required.
  • Communication and Presentation Skills: Strong written and verbal communication skills, including presentation skills, are required.

About Genmab:

Genmab is an international biotechnology company with a core purpose guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics.

We're committed to fostering workplace diversity at all levels of the company and believe it's essential for our continued success.

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