Medical Science Liaison - Remote

5w1 month ago

Pharmavise Corporation

Remote · Contract · $140,000 – $180,000

About this role

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. This field-based role bridges scientific knowledge with strategic business insights, ensuring alignment with corporate objectives while advancing scientific exchange and education.

Day-to-day responsibilities include establishing and maintaining relationships with KOLs, investigators, and other stakeholders in the healthcare and research communities. The MSL serves as a subject matter expert to deliver accurate, fair-balanced, and evidence-based scientific and clinical information regarding company products and pipeline.

The MSL collaborates with cross-functional teams including R&D, marketing, and regulatory to inform strategy and planning. This role also supports clinical trial activities by identifying potential sites, assisting with feasibility assessments, and maintaining communication with study investigators.

This remote position offers the opportunity to work independently while contributing to the company's scientific leadership. The MSL will monitor and report competitive intelligence and therapeutic landscape changes, ensuring compliance with all internal and external policies and regulations.

Requirements

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

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.