Jobs · Research

Medical Science Liaison - Neurology West (WA, OR, CA, NV, AZ, CO, NM, WY)

Lantheus · California, United States · 1 mo ago
RemoteRemoteResearch$156k–$234k/yrFull-time

About the role

Lantheus is a radiopharmaceutical-focused company dedicated to enabling clinicians to Find, Fight and Follow disease for better patient outcomes. As a Medical Science Liaison (MSL) at Lantheus, you will serve as a field-based scientific expert and key member of Global Medical Affairs, building trusted peer-to-peer relationships with healthcare professionals, KOLs, investigators, academic institutions, and other stakeholders. The role involves facilitating balanced, evidence-based scientific exchange, generating medical insights, and supporting medical strategy to improve patient outcomes. This is a remote position open to applicants authorized to work for any employer within the United States. Preferred candidates will reside near a major international airport.

Responsibilities

  • Scientific Engagement:
    • Develop, cultivate, and maintain strategic long-term scientific relationships with KOLs, investigators, healthcare professionals, academic institutions, and professional societies.
    • Conduct high-quality, peer-to-peer scientific exchange using current evidence to communicate approved scientific, clinical, and technical information regarding disease state, diagnostic imaging, radiopharmaceuticals, clinical trial data, treatment guidelines, and emerging scientific evidence.
    • Present complex scientific information effectively in one-on-one and group settings, tailoring communications to diverse audiences while maintaining scientific accuracy and compliance.
    • Respond to unsolicited scientific and medical information requests by providing timely, balanced, accurate, and evidence-based information in accordance with company policies and regulations.
    • Maintain advanced scientific expertise in therapeutic area, radiopharmaceuticals, molecular imaging, clinical trial data, and evolving therapeutic landscapes.
  • Medical Insight Generation:
    • Proactively gather, document, and communicate actionable medical insights from external expert interactions.
    • Identify emerging scientific trends, diagnostic imaging patterns, treatment advances, unmet medical needs, competitive intelligence, healthcare system challenges, and evolving standards of care.
    • Provide strategic field intelligence to inform Medical Affairs strategy, evidence generation priorities, product lifecycle management, and future research initiatives.
    • Communicate actionable insights to Medical Affairs leadership and cross-functional partners including Clinical Development, Clinical Operations, Commercial, Regulatory Affairs, Market Access, and Health Economics.
  • Congress and Scientific Meeting Support:
    • Represent Medical Affairs at national, regional, and international scientific congresses, professional society meetings, and educational conferences.
    • Develop and execute strategic congress engagement plans, including priority KOL interactions, scientific sessions, and educational opportunities.
    • Facilitate compliant scientific discussions with healthcare professionals before, during, and after scientific meetings.
    • Collect, analyze, and disseminate key scientific updates, competitive intelligence, clinical data, and emerging research findings to internal stakeholders.
    • Prepare congress summaries and scientific debriefs to support organizational learning and medical strategy.
  • Clinical Research and Study Support:
    • Identify and evaluate qualified investigators and clinical research sites for company-sponsored and investigator-sponsored studies.
    • Support clinical trial feasibility assessments, investigator identification, site engagement, and evidence generation initiatives.
    • Facilitate scientific collaboration between investigators and internal clinical development teams while maintaining appropriate separation from operational trial management.
    • Support investigator-sponsored research (ISR), post-marketing studies, real-world evidence initiatives, and collaborative scientific research opportunities.
    • Demonstrate comprehensive knowledge of clinical trial design, Good Clinical Practice (GCP), and clinical research methodology.
  • Medical Education and Scientific Communication:
    • Deliver scientific and educational presentations to healthcare professionals and internal stakeholders on disease state, radiopharmaceuticals, oncology, diagnostic imaging, clinical evidence, and emerging data.
    • Support advisory boards, speaker development, educational initiatives, scientific roundtables, and medical education programs.
    • Provide constructive scientific feedback regarding presentation accuracy, scientific content, and compliance with company policies.
    • Serve as a scientific resource to internal cross-functional teams by providing therapeutic area expertise and medical education.
  • Cross-Functional Collaboration:
    • Collaborate effectively with Medical Affairs, Clinical Development, Commercial, Regulatory Affairs, Market Access, Pharmacovigilance, Health Economics, Professional Promotions, and other cross-functional partners.
    • Share appropriate clinical, scientific, and technical information in a timely manner to support organizational objectives.
    • Contribute scientific expertise to product launches, lifecycle management activities, publication planning, evidence generation, and strategic initiatives.
  • Compliance and Pharmacovigilance:
    • Comply with Lantheus Pharmacovigilance procedures, including timely identification, documentation, and reporting of adverse events and product quality complaints.
    • Conduct all activities in accordance with the Lantheus Code of Conduct, Medical Affairs policies, OIG Guidance, PhRMA Code, GCP, HIPAA, FDA regulations, and all applicable legal and ethical standards.
    • Accurately document scientific interactions, field medical activities, and medical insights using approved systems and processes.
    • Maintain current knowledge of evolving scientific literature, treatment guidelines, regulatory requirements, and compliance expectations.

Requirements

  • PhD, PharmD, MD, DO, or equivalent advanced scientific or clinical degree required.
  • Minimum of two years of Medical Science Liaison or Medical Affairs experience preferred.
  • Clinical or scientific experience in therapeutics area, nuclear medicine, radiopharmaceuticals, molecular imaging, or diagnostic imaging preferred.
  • Demonstrated understanding of current and emerging trends in therapeutic area, radiopharmaceuticals, precision medicine, and diagnostic imaging.
  • Strong scientific acumen with the ability to critically evaluate and communicate complex clinical and scientific information.
  • Proven ability to establish and maintain credible scientific relationships with healthcare professionals and external experts.
  • Demonstrated leadership within cross-functional teams and the ability to collaborate effectively across multiple business functions.
  • Excellent verbal, written, presentation, and interpersonal communication skills.
  • Highly organized with demonstrated ability to independently manage multiple priorities in a dynamic environment.
  • Strong analytical thinking, strategic planning, and problem-solving capabilities.

Preferred Qualifications

  • Advanced knowledge of therapeutic area, radiopharmaceuticals, molecular imaging, and precision medicine.
  • Strong familiarity with key clinical publications, treatment guidelines, and evolving scientific literature.
  • In-depth understanding of clinical trial design, clinical development, and evidence generation.
  • Knowledge of investigator-sponsored research, real-world evidence, and post-marketing research.
  • Understanding of pharmacoeconomic principles and healthcare value evidence.
  • Advanced knowledge of the U.S. healthcare system, reimbursement environment, and medical imaging industry.
  • Experience supporting scientific congresses and advisory boards.
  • Advanced proficiency with Microsoft Office Suite (Word, Excel, PowerPoint) and CRM/documentation platforms.
  • Ability to travel approximately 70% within the assigned geography.
  • Residence near a major international airport preferred.

Benefits

  • Comprehensive health benefits package including medical, prescription drug, dental, and vision coverage.
  • Life and disability benefits.
  • Pre-tax accounts.
  • 401(k) with company contribution.
  • Generous time off package including paid vacation, holidays, sick days, and paid parental leave.

Pay

The pay range for this position is between $156,000 and $234,000 annually. Actual base pay offered may vary depending on job-related knowledge, skills, and experience. Employees in this position are eligible for a discretionary performance-based cash incentive.

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