Medical Science Liaison

🕒 May 20

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

👻 Ghost score 42%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Pharmavise Corporation

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2013

💼 Consulting

📦 Logistics

🏭 Manufacturing

Consulting • Logistics • Manufacturing

Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.

📋 Description

• 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.

🎯 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. • 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.

🏖️ Benefits

• paid holidays • Paid Time Off (PTO) policy • medical insurance