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Director, US Medical Affairs, Hematology

Employer
Genmab
Location
Princeton, New Jersey (US)
Salary
Highly competitive salary, incentives, and new hire equity grant. No-cost medical benefits.
Closing date
Jun 19, 2022

View more

Position
Medical Director
Category
Hematologic Oncology
Hours
Full Time
Education
MD, MD / PHD

Job Details

The Director, US Medical Affairs, Hematology will be the subject matter expert responsible for providing medical needs to the development and execution of the US Medical Affairs strategic and tactical plans and support the US medical launch planning, and execution for epcoritamab in close alignment and collaboration with the US Medical Affairs Strategy Lead. This role will report to the Senior Director, US Medical Affairs, Hematology (US Medical Affairs Strategy Lead)

 

Job Responsibilities

 

As an integral part of the US Oncology Medical Affairs Team, and in close collaboration with the US MASL and cross-functional partners, the Director, US Medical Affairs Hematology will establish and maintain the relationships with the US Key Opinion Leaders and other prioritized external stakeholders.

 

 

 

In addition, the Director, US Medical Affairs Hematology will have commercial aptitude and/or experience, including proven ability to translate and align commercial and scientific goals and objectives.

 

He/She will advise on the development of US medical education, publications, and various medical communication tactics.  He/she will partner with internal stakeholders to address learning and development needs for the organization related to the TA. He/She will provide input and strategic direction on data generation and life cycle management initiatives.

 

Specific responsibilities for this role will include but are not limited to:

 

  • Participate in the development and execution of US Medical Affairs Strategy and Plan
  • Provide medical monitoring and medical oversight for company sponsored Medical Affairs led interventional and observational clinical trials and real-world data generation
  • Support cross-functional launch activities
  • Prepare and educate internal and external stakeholders on disease, treatment landscape and asset
  • Serve as a medical and content expert for internal and external stakeholders
  • Play an integral role in the planning and execution of US advisory boards
  • Represent Genmab at key Global and US medical conferences/meetings
  • Ensure global and US cross functional collaborations and partnerships to align as One Genmab
  • Provide scientific input and strategic direction to the medical affairs data generation plan, including investigator-sponsored trial (IST)/collaborative studies program for an asset/disease
  • Lead the execution of the pre-approval access program for hematology
  • Provide input for Medical and Promotional Review Committees
  • Provide scientific/medical input into local regulatory/reimbursement/policy related documents and interactions

Requirements:

 

  • A doctoral degree is required; MD is preferred
  • Relevant experience in medical affairs, health outcomes, clinical and or translational research in hematology or oncology with 5+ years of academic, clinical practice, and or industry experience highly preferred
  • Industry experience desirable, including recent experience of a successful pre-launch or launch experience within Oncology and/or Hematology
  • Ability to think medically and strategically about the short-, mid- and long-term impacts within the oncology health care landscape
  • Ability to lead collaboratively across various internal stakeholders and develop trusted partnerships
  • A strong ability to interpret and articulate clinical/translational/health economics outcomes research data as well as the oncology clinical development program vision
  • Good understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D and Commercial work
  • Fair knowledge of evidence-based medicine concepts, applied biostatistics and health economics are desirable
  • Demonstrated organizational skills to manage multiple projects simultaneously
  • Strong written and verbal communication skills (including presentation skills) along with excellent judgment and ability to work in a matrix team environment
  • Ability to travel to US and occasionally international conferences and meetings, which will include occasional weekend travel

Company

Be part of the extra[not]ordinary™

Are you caring, candid, impact-driven and determined to make a difference? Join our unstoppable team as we improve the lives of patients through innovative and differentiated antibody therapeutics.

About Genmab

Founded in 1999 in Copenhagen, Denmark, Genmab is an innovative biotech company that has become a leader in antibody biology and innovation. Our product pipeline and next-generation antibody technologies are the result of our strong company culture, a deep passion for innovation, and desire to transform cancer treatment and serious diseases.

When you work with us, you’ll be part of a warm, fun, dynamic community, and team up with some of the best, most authentic individuals in locations around the world, who care deeply and share in a relentless drive to innovate and create transformational medicines. People who are candid, impact-driven, and a little unconventional; who seek out and embrace the opportunity to build new and bold futures within a rapidly growing and innovative biotech company; who bring their full selves to work and show up for each other - rolling up their sleeves to get the job done. This translates into a place where you can be authentically you; are empowered to innovate, build solutions, and execute; feel cared for and supported in growth; and are a critical part of changing the lives of patients around the world through transformative cancer treatment.

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