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Description

The Medical Information Specialist is responsible for supporting the medical information needs of healthcare professionals, patients, and internal stakeholders. The role will contribute to the development and management of high-quality medical content, such as Standard Response Letters (SRLs), Frequently Asked Questions (FAQs), and maintains product- and disease-specific scientific repositories. The role also ensures compliance with regulatory standards, collaborates cross-functionally with internal teams such as Drug Safety and Medical Science Liaisons (MSLs), and provides operational support through tracking, reporting, and database management.

Essential Functions:

Medical Inquiry Management & MIRF Triaging: Ensures timely, accurate, balanced, and compliant responses to unsolicited medical inquiries received from healthcare

professionals, patients, and internal stakeholders. Supports inquiry fulfillment via field team requests and the call center. Triages and manages Medical Information Requests (MIRFS) from healthcare professionals. Ensures timely, accurate, and compliant responses are delivered, and documents all inquiries in tracking systems per SOPs.

Medical Information Content Development and Maintenance: Maintains and updates Standard Response Letters (SRLs), FAQs, and product/disease-state repositories to support medical inquiry responses. Ensures content is aligned with current product labeling and scientific data. Ensures version control and repository updates for scientific and operational documents.

Operations and Compliance Support: Supports operational tasks including documentation for grants and IITs, vendor coordination, and purchase order tracking. Assists with vendor onboarding and supports systems related to Medical Information operations, including tracking purchase orders (POs), contracts, and budget documentation. Assists in ensuring audit readiness and compliance across all Medical Information activities.

Medical Information Database Management: Oversees medical information databases and inquiry tracking tools. Analyzes trends in inquiries and prepares reports to communicate actionable insights to internal stakeholders. Internal Collaboration & Stakeholder Support: Collaborates with MSLs, Drug Safety, and

internal teams to ensure consistent scientific messaging. Submits scientific materials for internal review (e.g., SERC), ensuring all supporting documentation is included and

compliant

Skills

Pharmd, Medical affairs, medical inquiries, medical inquiry, global, standard response letter, medical writing

Additional Skills & Qualifications

Education:

Doctorate Degree / Advanced degree (PharmD, PhD or MD in relevant discipline)

Experience:

1–3 years of experience in Medical Information, Medical Writing/Medical Affairs or other relevant functions in the pharmaceutical, healthcare, or life sciences industry.

Skills:

Demonstrated expertise in medical information communication & management -

Excellent verbal and written communication skills and interpersonal skills

Excellent organization skills, task-oriented and strong attention to detail and deadlines -

Ability of engage collaboratively with stakeholders

Expertise in Microsoft Office, Teams, and Veeva Vault Systems

Literature database search skills

Understanding of global regulatory, legal and compliance requirements

This is a hybrid position in Bridgewater,NJ. (must be on-site 3 days/week)

Application Deadline

This position is anticipated to close on Oct 20, 2025.

Pay and Benefits

The pay range for this position is $90000.00 - $110000.00/yr.

The base salary for this position ranges from $95,000 to $110,000 per year. In addition, offers a short-term incentive opportunity, such as a bonus or performance-based award

Workplace Type

This is a hybrid position in Bridgewater,NJ.

Application Deadline

This position is anticipated to close on Oct 20, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.