Remote Medical Science Liaison

Purpose and Scope

 The Medical Science Liaison (MSL), Oncology and Men’s Health, is a field-based medical affairs professional responsible for advancing high-quality, non-promotional scientific exchange with external experts, healthcare professionals, and other stakeholders. The role serves as a trusted scientific resource across oncology and men’s health and additional therapeutic areas as the company grows. In this role you will support the Medical Affairs team and cross-functional brand partners by participating in evidence-based decision-making, identifying medical, scientific and clinical insights in a timely fashion and contribute to medical strategy across the product lifecycle.

The ideal candidate has brings strong scientific, medical or clinical expertise, excellent communication skills, experience with publications or scientific content development, and a commitment to compliant, accurate, and timely medical information support.

Essential Duties & Responsibilities

Scientific Engagement and External Stakeholder Management

• 
  
• Develop and maintain peer-to-peer scientific relationships with key opinion leaders, healthcare professionals, investigators, academic centers, and relevant professional organizations.
  
• Deliver balanced, accurate, and non-promotional scientific exchange on disease state, clinical data, real-world evidence, treatment pathways and guidelines, and unmet needs in oncology and men’s health.
  
• Identify, gather, and communicate actionable medical insights to inform medical strategy, evidence generation, education priorities, and cross-functional planning.
  
• Support advisory boards, congress activities, speaker development, educational initiatives, and investigator engagement in accordance with applicable policies, regulations and brand needs in a timely fashion.
  

Publications and Scientific Content Support

• 
  
• Monitor evolving research, congress updates, treatment trends, and stakeholder perspectives to identify implications for medical strategy and patient care.
  
• Translate complex clinical and scientific evidence into clear, audience-appropriate discussions while preserving scientific integrity and compliance.
  
• Contribute to publication planning activities, including identification of evidence gaps, congress abstract opportunities, manuscript concepts, manuscript development and data communication opportunities.
  
• Collaborate with medical affairs, clinical, biostatistics, and external authors to support development of abstracts, posters, manuscripts, slide decks, and scientific communication materials.
  
• Review scientific content for accuracy, balance, clarity, and alignment with approved data, product label and publication standards.
  
• Support interpretation and communication of clinical trial results, real-world evidence, health outcomes research, and investigator-sponsored research outputs.
  

Medical Information Support

• 
  
• Serve as a dedicated scientific resource for medical information support, including development, review, and maintenance of standard response documents, frequently asked questions, medical letters, and scientific background materials.
  
• Respond to escalated or complex unsolicited medical inquiries from healthcare professionals in a timely, accurate, balanced, and compliant manner.
  
• Collaborate with medical information, pharmacovigilance, regulatory, legal, and commercial colleagues to ensure responses are scientifically rigorous and aligned with company policies.
  
• Identify recurring inquiry trends and communicate insights to inform medical education, field training, content development, and evidence-generation priorities.
  

Internal Collaboration and Compliance

• 
  
• Partner with medical affairs leadership and cross-functional teams to execute medical plans, field strategy, training initiatives, and evidence dissemination activities.
  
• Support internal training activities by developing and delivering scientific training, disease-state education, product data updates, congress debriefs, and medical information process guidance for internal stakeholders.
  
• Provide ongoing scientific updates to ensure organizational understanding of therapeutic area developments, clinical data, stakeholder insights, and implications for medical strategy.
  
• Operate with the highest standards of ethics, scientific integrity, and compliance with applicable laws, industry codes, company policies, and non-promotional medical affairs practices.
  
• Document activities, insights, project outcomes, and stakeholder engagements accurately and in accordance with company requirements.<