Medical Science Liaison - New England

Medical Science Liaison

Our client offers a collaborative network supporting an innovative pipeline across multiple therapeutic areas, including inflammation. As a Regional Medical Science Liaison, you will drive clinical program execution, foster connections with the medical community, communicate scientific and clinical information, and collect insights to inform strategic objectives.

Role Overview

As an Amplity employee, you will support Medical Affairs on behalf of our client. You will interface clinical trial sites, collaborate, and engage opinion leaders to communicate non‑promotional scientific and medical information across our client’s portfolio.

Core Responsibilities

• Clinical Trial Support: Serve as the primary interface with clinical trial sites, collaborating with Clinical Development and Operations to ensure high‑quality study execution. Participate in planning and setup for your region, aligning with local colleagues and CROs.
• Scientific Expertise: Develop deep expertise in multiple therapeutic areas, including inflammatory bowel disease. Act as the regional subject matter expert and credible scientific leader.
• Opinion Leader Engagement: Build and maintain relationships with opinion leaders, clinical investigators, and study staff within your region.
• Cross‑Functional Support: Provide scientific support to Clinical Development, Medical Affairs, Commercial, and other teams. Support activities such as local, regional, national, and as needed, international congresses. Share clinical and scientific insights with cross‑functional teams.
• Compliance: Operate ethically and comply with all laws, regulations, and policies.

Qualifications

• Minimum master’s degree with medical credential (NP, RN, PA) from an accredited institution.
• Terminal degree (PharmD, PhD) highly preferred.
• MSL with pharmaceutical experience and medical credential (RN) may be considered with bachelor’s degree.
• MSL experience required (minimum 2‑3 years) with drug pre‑approval (pre‑PDUFA).
• IBD/GI or immunology experience strongly preferred.
• Strong written and verbal communication skills; ability to present medical/scientific information clearly.
• Relationship‑building and networking skills.
• Excellent organization and results orientation.
• Influence and negotiation skills.
• Ability to work independently and in teams in a dynamic environment.
• Experience with clinical trial design, conduct, and evaluation.
• Permanent residence within assigned region. Ability to travel 70% of the time.
• Proficiency with Microsoft Suite and digital meeting platforms.
• Safe driving record and valid driver’s license required.

Benefits

• Competitive base salary and bonus potential $200K - $230K.
• Generous PTO and paid holidays.
• 401K, medical, dental, vision coverage.
• Company‑funded wellness program, long‑term/short‑term disability, life insurance.

EEO Statement

We encourage and support equal employment opportunities for all associates and applicants for employment without regard to sex, race, color, religion, national origin, age, disability, marital status, sexual orientation or veteran status. Employment decisions are evaluated on the basis of an individual's skills, knowledge, abilities, job performance and other qualifications.