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Director, Global Medical Communications

Job in Springfield, Hampden County, Massachusetts, 01119, USA
Listing for: Karyopharm Therapeutics Inc.
Full Time position
Listed on 2026-06-26
Job specializations:
  • Healthcare
    Medical Imaging
Job Description & How to Apply Below

Role Overview & Key Functions:

The Director of Medical Communications will be a member of the Global Medical and Scientific Affairs team. Reporting to the Head of Medical Communications/Publications, the candidate will be responsible for developing and delivering high quality oncology medical communication training pieces (print/digital) in a cross-functional environment across a variety of tumor types. The role supports the following strategic imperatives:

  • Build awareness of Karyopharm’s clinical programs and scientific leadership in the field of Oncology
  • Support the differentiation of Karyopharm from competitors
  • Lead the generation and dissemination of data to educate HCP and other relevant audiences
  • Build strong relationships and collaborations with KOLs and/or principal investigators with initiatives that make Karyopharm a leader with science, innovation, and patient focused activities.
RESPONSIBILITIES:

Medical Communications:

  • Provide strategic leadership to Medical Communications in support of the oncology field including, but not limited to, educational and training materials for relevant diseases and products.
  • Create scientific tools and materials in support of the oncology business including, but not limited to educational/training materials, disease state and product slide kits, etc.
  • Develop scientific programs and materials for internal and external stakeholders.
  • Manage the work of external medical communication vendors, providing specific guidance on projects, as well as timeliness and quality of deliverables and adherence to budget.
  • Act as liaison to field-based medical affairs to produce high-quality and useful communication tools, slide decks, and training programs.
  • Lead the development of high-quality and high-impact scientific content in support of medical affairs, clinical development and other internal stakeholders.
  • Contribute to the development, review, and/or refinement of clinical content for advisory boards and investigator meetings.
  • Orchestrate the development of a strategic scientific communication tools, including study data compendia and treatment guideline plan summaries.
  • Ensure awareness of current trends within the industry, identify benchmarks and establish “best practices” within the function.
  • Incorporate tools and strategies that ensure cutting-edge innovation in scientific communications, while remaining in compliance to all policies and regulations.
  • Evaluate adherence to policies and/or procedures and implement corrective action when needed.
  • Conduct business in accordance with Karyopharm values.
  • Provide clinical and/or scientific information, input and interpretation, as needed.
  • Serve as a scientific/clinical content reviewer for communication pieces developed and ultimately submitted to the legal, medical regulatory review team.
  • Partner with the Brand team to deliver and/or review scientific content for commercial deliverables.
  • Create new training materials, and update existing training materials, as needed.
  • Partner with MSL Director on MSL training, both for new hires and for ongoing training work streams.
  • Assess competency of MSLs with MSL Director.
  • Coordinate live and Web-based training meetings for internal stakeholders.
  • Become a content expert that can deliver training presentations/sessions.
  • When applicable, coordinate new hire and ongoing training for other GMSA employees, outside of the MSL team.
  • Partner with the other team members on deliverables which include congress planning, congress materials, and other GMSA tools and resources.
  • Partner with Sales Training on clinical content of sales training materials.
  • Help create pre-congress materials (briefing books, content analysis etc.), congress sessions coverage and reporting plan and post-congress executive summary report.
  • Lead the execution of these plans through a cross functional team setting.
Candidate Profile & Requirements:
QUALIFICATIONS:
  • Advanced degree in a related scientific or clinical discipline (MD, PharmD, or PhD) with at least 5 years’ relevant experience in the pharmaceutical or biotechnology industry in Medical/Scientific Communications.
  • Oncology training or experience in solid and/or hematologic malignancies…
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