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Omeros

Biopharmaceuticals discovering, developing, commercialising therapeutics

Regional Medical Science Liaison - Midwest

Biology & BiotechConfirmed live in the last 24 hours
Full-timeUnited States

About the Job

Requirements

  • An advanced clinical/science degree or professional credential (PharmD, PhD, or MD), or equivalent, is required.
  • A minimum of 3 years of previous experience as an MSL in the biotechnology or pharmaceutical industry is required.
  • Demonstrated knowledge of regulatory, commercial, and clinical issues affecting the pharmaceutical industry is required.
  • Verbal and written communication, presentation, and interpersonal skills are required.
  • Planning, organizational, and project management abilities are required.
  • Ability to collaborate in a team environment and partner effectively across geographic areas and cross-functional groups is required.
  • A dependable automobile with liability insurance and a valid driver's license is required.
  • Candidates should be located in ND, SD, MN, IA, WI, IL, MI, IN, OH, or KY.
  • The employee must undertake extensive overnight travel (50–75%).
  • The employee must be able to perform intermittent physical activity including bending, reaching, pushing, pulling, or lifting up to 40 lbs., and may encounter prolonged periods of sitting.
  • The employee must conduct activities in accordance with applicable legal, regulatory, and corporate requirements, including the company Code of Business Conduct & Ethics, policies, and procedures.

Responsibilities

  • Build and foster professional relationships and partnerships with core local, national, and international key opinion leaders in medical education and clinical/scientific research, serving as a key clinical and scientific resource.
  • Maintain thorough and up-to-date knowledge of disease states, clinical information, and product data within relevant therapeutic areas.
  • Implement strategies and tactics aligned with the overall medical strategy and plan to communicate complex scientific education, including disease-state and product information.
  • Deliver medical and scientific presentations to physicians, pharmacists, nurses, payers, and internal staff.
  • Contribute to the development and implementation of publication planning, medical education strategies, initiatives and materials, and standard response letters.
  • Facilitate submission and discussion of independent investigator-initiated studies as a conduit between investigators and the internal Omeros IIS committee.
  • Contribute to the development of medical affairs materials such as slide decks, abstracts, and manuscripts.
  • Identify opportunities to partner with key opinion leaders on disease-state or therapeutic initiatives.
  • Support and facilitate speaker-training initiatives.
  • Collect, analyze, and interpret disease-state and technical product information at medical congresses.
  • Provide clinical/scientific education for Sales & Marketing staff.
  • Partner and collaborate with Clinical Development, Clinical Operations, Pharmacovigilance, and Sales & Marketing.
  • Support clinical development activities through site identification, investigator recruitment, and education.
  • Support market-access initiatives, including engagement with or presentations to commercial and public payers, as needed.
  • Complete administrative responsibilities and internal projects as assigned in a timely and accurate manner.

Desired Qualifications

  • Clinical experience in neurology, oncology, immunology, or cardiovascular disease is desirable.
  • Experience in at least one start-up biopharma company is desirable.
  • Ability to think strategically and execute to deliver medical plans.
  • Ability to act professionally as an external company representative.
  • Ability to build and maintain positive relationships with management, peers, and subordinates.
  • Competent business writing and persuasive presentation skills.
  • Organizational management and problem-solving skills.
  • Ability to manage multiple projects, therapeutic areas, and external and internal relationships.

About the Company

Omeros

Biopharmaceuticals discovering, developing, commercialising therapeutics

Omeros develops medicines that target the body's complement system, using both small-molecule drugs and biologics. Its lead drug narsoplimab (Yartemlea) is a monoclonal antibody that blocks MASP-2, and it was approved by the FDA in December 2025 for transplant-associated thrombotic microangiopathy (TA-TMA). The company also advances OMS906, a complement factor D inhibitor studied for diseases like paroxysmal nocturnal hemoglobinuria. Its goal is to provide therapies for complement-driven diseases and broaden its portfolio, including ongoing European regulatory reviews.

Company size
201-500
Company stage
IPO
Headquarters
Seattle, WA
Founded
1994

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