Merus N.V. logo

Medical Science Liaison (Central)

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

Role Summary

Medical Science Liaison (MSL) responsible for engaging with Healthcare Professionals (HCPs) in their territory through high-level scientific support for education and scientific exchange. The MSL will be a conduit for medical affairs communications and interactions with assigned HCPs. Knowledge of oncology is required; knowledge of NGS testing and companion diagnostics is preferred. Central US location preferred.

Responsibilities

  • Support study start-up through review of competitive trial landscape, precedent trials; leverage contacts in the medical community with prospective PIs, engagement and follow-up with potential sites
  • Expand knowledge of investigational sites, both current and new, to build a network including site capabilities and past performance
  • Inform Clinical Operations when an investigator expresses interest in becoming a site
  • Develop and execute field medical affairs plan for the assigned territory in alignment 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
  • Provide complete and timely documentation of interactions and contacts
  • Complete administrative reports such as expense and status reports in a timely manner
  • Provide reports, assessments and HCP insights in a clear, succinct and timely fashion
  • Maintain and continually develop scientific knowledge of the relevant competitive landscape
  • Attend and participate in all required compliance trainings
  • Follow all laws, rules, regulations, guidance documents and codes applicable to the pharmaceutical industry
  • Attend national, regional and local conferences and symposia in coordination with overarching company objectives
  • Follow all company policies and procedures as well as those applicable to collaborators and institutions

Qualifications

  • Required: M.D., Ph.D., Pharm.D. or NP/PA with appropriate clinical experience and scientific background
  • Required: 2+ years oncology clinical experience and 1+ years MSL experience in the pharmaceutical industry
  • Required: Knowledge of pharmaceutical rules, regulatory law, guidelines and codes (e.g., PhRMA Code)
  • Required: Strong collaboration skills to coordinate efforts and accomplish goals as a team
  • Required: Demonstrate ability to develop trust and maintain integrity with internal and external partners, peers, and others
  • Required: Excellent interpersonal, verbal and written communication skills
  • Required: Ability to learn new scientific and technical information quickly
  • Required: Strong computer skills, proficiency in on-line data searches, MS Word, PowerPoint & Excel
  • Required: Ability to handle and prioritize multiple assignments and meet deadlines in a fast-paced environment
  • Preferred: Knowledge of oncology beyond core field and experience with NGS testing and companion diagnostics

Skills

  • Strong communication and presentation skills
  • Analytical thinking and problem-solving capabilities
  • Collaborative approach to cross-functional teamwork
  • Comfort with travel and field-based roles

Education

  • MD, PhD, PharmD or NP/PA with appropriate clinical experience and scientific background

Additional Requirements

  • Travel approximately 50% (car, plane, etc.)
Apply now
Share this job