Medical Science Liaison

Job Summary:

The Medical Science Liaison (MSL) serves as a scientific expert responsible for building and maintaining strong relationships with key opinion leaders (KOLs), healthcare professionals, and academic researchers. The MSL provides in-depth scientific and clinical knowledge to support the safe and effective use of the company’s products across therapeutic areas. This field-based role bridges scientific knowledge with strategic business insights, ensuring alignment with corporate objectives while advancing scientific exchange and education.

Key Responsibilities:

• Establish and maintain relationships with KOLs, investigators, and other stakeholders in the healthcare and research communities.
  

• Serve as a subject matter expert to deliver accurate, fair-balanced, and evidence-based scientific and clinical information regarding company products and pipeline.
  

• Support clinical trial activities by identifying potential sites, assisting with feasibility assessments, and maintaining communication with study investigators.
  

• Provide medical insights to cross-functional teams (e.g., R&D, marketing, regulatory) to inform strategy and planning.
  

• Respond to unsolicited medical inquiries from healthcare providers in compliance with regulatory and legal requirements.
  

• Deliver medical education presentations to healthcare professionals in both individual and group settings.
  

• Collaborate with internal teams on scientific communications, including publications, congress materials, and advisory board content.
  

• Monitor and report competitive intelligence and therapeutic landscape changes.
  

• Ensure compliance with all internal and external policies, regulations, and SOPs, including those related to interactions with healthcare providers.
  

Minimum Qualifications:

• Advanced degree (PharmD, MD, PhD) in a relevant scientific discipline required.
  

• 2–5 years of experience as an MSL or in a similar medical affairs/scientific role within the pharmaceutical, biotech, or life sciences industry.
  

• Strong knowledge of clinical trial design, regulatory guidelines, and scientific literature evaluation.
  

• Excellent communication and interpersonal skills; ability to translate complex scientific data into compelling insights for diverse audiences.
  

• Demonstrated ability to build trust and credibility with external stakeholders.
  

• Proficient in using CRM tools, MS Office Suite, and virtual meeting platforms.
  

• Ability to travel up to 50–70% domestically, with occasional international travel as needed.
  

• 
  

In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth.

E-Verify Participation:

Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at or through their website at dhs.gov/e-verify.