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Associate Director, Medical Affairs Strategy (1 year Contract)

Employer
Genmab
Location
Working from home
Salary
Highly competitive salary, incentives, and new hire equity grant. No-cost medical benefits.
Closing date
Jun 18, 2022

View more

Position
Director
Category
Biotechnology
Hours
Full Time
Education
MD / PHD, MS, NP, BS, BSN
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The Associate Director, Medical Affairs Strategy will provide scientific/medical support for Genmab compounds in various stages of clinical development.  This individual will oversee the competitive oncology landscape in areas of interest to Genmab and keep cross-functional teams abreast of the insights and impact to clinical programs. He/she will serve as oncology therapeutic areas expert in content creation, tactical discussions, and presentations with internal colleagues. In addition, the individual will also work closely with commercial teams as well as closely collaborate with clinical development/operation on Medical Affairs support of priority trials.

 

This is a one-year contract with flexibility to work remotely.

 

Responsibilities

 

Responsibilities will include, but are not limited to, the following:

 

  • Lead the competitive insights coverage on regular basis and at congresses and contribute to scientific review and interpretation of key competitive data presentation and provide key implications to Genmab products to cross-functional teams
  • Contribute to congress and local professional meeting scientific coverage and reports
  • Support the execution of the Global medical affairs strategy and tactics for Genmab assets
  • In close collaboration with Field Medical Affairs, contribute to the development of a disease area/trial Engagement Plan, including engagement plans for congresses and professional meetings
  • Provide support for Medical Affairs cross-functional working groups
  • High quality scientific/clinical input and review of:  abstracts, posters, slides, manuscripts in disease area, educational materials in disease area including slides, webcasts, etc., advisory board meeting objectives and materials, booth panels, Med info letters, and promotional materials
  • Contribute and assist in delivering relevant training and materials for the broader Medical Affairs teams, globally

 

 

Requirements

 


Moreover, you meet the following professional requirements:

 

  • Advanced degree (MS, PhD, MD) preferred in medicine, immunology/biology or other relevant life sciences area preferred.
  • Experience in medical affairs and clinical research in oncology
  • Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.
  • Proficiency in scientific and clinical data review and interpretation.
  • Strong organization skills.
  • Knowledge/application of data sources, reports and tools for the creation of solid plans.
  • • Ability to work successfully under pressure in a fast-paced environment and with tight timelines
  • • Ability to be proactive, enthusiastic and goal orientated
  • • A team player with demonstrated ability to collaborate with a diverse group of internal and external stakeholders to support product development strategy
  • • Strong communication skills - both oral and written
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