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Field Medical Science Liaison

Job in Tampa, Hillsborough County, Florida, 33646, USA
Listing for: Nobelpharma America, LLC
Full Time position
Listed on 2026-07-14
Job specializations:
  • Science
    Medical Science Liaison
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR
Job Description & How to Apply Below

At Nobelpharma America, LLC, the Medical Science Liaison (MSL) is a field‑based scientific expert and key extension of the Medical Affairs organization. This position involves frequent travel (up to 50%–75%) across southeastern, midwestern, and southern regions.

Key Responsibilities Scientific Engagement & External Partnerships
  • Build and maintain strong, credible, long‑term relationships with key opinion leaders (KOLs), specialists, investigators, patient advocacy organizations, and centers of excellence across assigned territories.
  • Conduct high‑quality scientific exchange with external stakeholders to communicate clinical data, disease‑state information, treatment insights, and emerging research in a fair and balanced manner.
  • Identify, map, and prioritize key stakeholders in alignment with medical strategy and organizational objectives.
  • Represent Nobelpharma America, LLC at scientific congresses, educational programs, advisory activities, and medical meetings.
Medical Support & Scientific Expertise
  • Maintain a high level of clinical, scientific, and technical expertise in relevant therapeutic areas and company‑supported products.
  • Deliver compliant, non‑promotional scientific presentations and educational support to external experts and internal stakeholders.
  • Respond to unsolicited medical inquiries with timely, accurate, and evidence‑based information in accordance with company policy and compliance standards.
  • Support medical and clinical initiatives, including clinical trial awareness, site identification, and investigator‑initiated study activities, as appropriate.
Insights & Strategy
  • Gather, synthesize, and communicate field insights related to treatment patterns, unmet medical needs, scientific trends, and the competitive landscape.
  • Share actionable insights with internal stakeholders to inform medical strategy, evidence generation, and broader business planning.
  • Provide strategic perspective from the field to support ongoing Medical Affairs objectives and organizational priorities.
Cross‑functional Collaboration
  • Collaborate effectively with cross‑functional teams including Medical Affairs, Medical Information, Pharmacovigilance, Market Access, and Commercial Operations.
  • Support internal initiatives such as speaker training and sales training by ensuring scientific accuracy and appropriate clinical context.
  • Partner with field leadership and other customer‑facing roles while maintaining clear boundaries and full compliance with all applicable regulations and company policies.
Compliance & Professional Standards
  • Conduct all activities in accordance with legal, regulatory, ethical, and company compliance requirements.
  • Maintain current knowledge of scientific literature, treatment guidelines, health‑care trends, and developments within relevant therapeutic areas.
  • Perform additional duties and special projects as needed to support Medical Affairs and company priorities.
Education & Experience
  • Advanced scientific or clinical degree required, such as PharmD, PhD, MD, DO, or equivalent.
  • Minimum three years’ experience as an MSL in the biopharmaceutical industry.
  • MSL‑BC certification is highly desirable.
  • Expert scientific and pharmaceutical knowledge, with an emphasis in rare disease.
Skills & Competencies
  • Strong scientific acumen with the ability to interpret and communicate complex clinical and scientific data to a variety of audiences.
  • Excellent communication, presentation, and relationship‑building skills.
  • Ability to work independently, manage territory activities, and prioritize multiple initiatives in a field‑based environment.
  • Strategic mindset with strong analytical, problem‑solving, and insight‑generation capabilities.
  • High degree of professionalism, integrity, and commitment to compliant scientific exchange.
Preferred Qualifications
  • Experience engaging with advocacy organizations, specialty treatment centers, or academic institutions.
  • Understanding of clinical trial design, research processes, and the evolving regulatory environment.
  • Established network of relevant scientific or clinical relationships is a plus.
Travel Requirements
  • Field‑based role requiring frequent travel, including attendance at conferences, site visits, stakeholder meetings, and internal meetings. Travel may be up to 50%–75%, including some weekends, and varies based on territory and business needs.
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