Medical Science Liaison - Great Lakes

Amplity Health; Indiana (PA); Hybrid; USD 200,000 - 230,000; Full time

Benefits offered by this job

401K, medical, dental, vision coverage

Generous PTO and paid holidays

Wellness program and disability/life保险

Job summary

Amplity Health is seeking an experienced Regional Medical Science Liaison to drive clinical program execution and engage with the medical community across our client portfolio. You will interface clinical trial sites, communicate scientific information, and gather insights to inform strategic objectives.

The role focuses on inflammatory diseases with substantial regional travel. You will develop deep therapeutic expertise, build relationships with opinion leaders, and support cross-functional

Qualifications

• MSL with pharmaceutical experience and medical credential (RN) may be considered with bachelor’s degree.
• Minimum master’s degree with medical credential (NP, RN, PA) from an accredited institution.
• Terminal degree (PharmD, PhD) highly preferred.
• IBD/GI or immunology experience strongly preferred.
• Strong written and verbal communication skills; ability to present medical/scientific information clearly.

Responsibilities

• Serve as primary interface with clinical trial sites, collaborating with Clinical Development and Operations for region-specific study execution.
• Develop deep expertise in multiple therapeutic areas, including inflammatory bowel disease; act as regional scientific leader.
• Engage opinion leaders, clinical investigators, and study staff within your region.
• Provide scientific support to cross-functional teams and participate in conferences as needed.
• Operate ethically and comply with all laws, regulations, and policies.

Skills

Communication skills

Relationship building

Organization

Influence & negotiation

Independent work

Team collaboration

Clinical trial experience

MSL experience

Travel readiness

Education

Master’s degree with medical credential (NP, RN, PA)

PharmD or PhD preferred

Bachelor’s degree with MSL experience considered

Tools

Microsoft Office

Video conferencing platforms

Job description

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.