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Medical Science Liaison (Central)

Merus N.V.
Full-time
Remote friendly (Cambridge, MA)
United States
$156,000 - $234,000 USD yearly
Medical Affairs

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Role Summary

Medical Science Liaison (Central). Central US location preferred. Join Merus to support the development of novel bispecific antibody therapeutics within a cross-functional medical affairs organization. The MSL will engage with Healthcare Professionals to provide high-level scientific support, education, and scientific exchange in oncology, reporting to the Field Medical Director.

Responsibilities

  • Support study start-up through review of competitive trial landscape, precedent trials, and engagement with potential sites.
  • Expand knowledge of investigational sites to build a network including site capabilities and past performance.
  • Inform Clinical Operations when investigators express interest in becoming a site.
  • Develop and execute field medical affairs plans for the assigned territory aligned with medical affairs strategies and tactics.
  • Serve as a liaison for clinical and scientific information exchange with regional oncologists, pathologists, oncology nurses, NPs, PAs and pharmacists.
  • Deliver high-quality education and awareness presentations to ensure optimal patient care.
  • Obtain, assimilate, organize and report field insights concisely, clearly, and compliantly.
  • Provide timely, accurate, specific, and balanced responses to professional information requests in collaboration with medical communications.
  • Maintain complete and timely documentation of interactions and contacts; complete administrative and status reports promptly.
  • Provide reports, assessments and HCP insights in a clear and timely fashion.
  • Maintain and continually develop scientific knowledge of the relevant competitive landscape.
  • Attend and participate in all required compliance trainings; follow all applicable laws, regulations, codes, and guidance.
  • Attend national, regional and local conferences and symposia in coordination with company objectives.

Qualifications

  • M.D., Ph.D., Pharm.D. or NP/PA with appropriate clinical experience and scientific background.
  • 2+ years oncology clinical experience and 1+ years MSL experience in the pharmaceutical industry.
  • Knowledge of pharmaceutical rules, regulatory law, guidelines and codes (e.g., PhRMA Code).
  • Strong collaboration skills and ability to coordinate efforts as a team.
  • Demonstrated ability to develop trust and maintain integrity with internal and external partners and peers.
  • Ability to meet individual and team objectives and results.
  • Excellent interpersonal, verbal and written communication skills.
  • Ability to learn new scientific and technical information quickly.
  • Strong computer skills, proficiency in online data searches, MS Word, PowerPoint & Excel.
  • Ability to handle and prioritize multiple assignments and meet deadlines in a fast-paced environment.
  • Travel approximately 50% (car, plane, etc.).

Skills

  • Scientific communication
  • Stakeholder engagement
  • Strategic field medical planning
  • Data interpretation and field insights reporting
  • Compliance and regulatory awareness

Education

  • Advanced degree required as specified (MD, PhD, PharmD, or NP/PA).
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