Promotional Review Specialist

Promotional Review Specialist

Contract Type:

Contract

Location:

Mansfield - MA

Industry:

Contact Name:

Michael DeSa

Contact Email:


Contact Phone:


Date Published:

11-18-2025

Salary:

$75.00 - $85.00 Per Hour

Job ID:

37965

Title:  Promotional Review Specialist
Job Type:  Contract
Contract Length:  6+ Months (potential for extension)
Target Start Date:  ASAP
Work Location/Structure:  Remote

About the Opportunity:

Our client, a leader in Medical Devices, is looking for a skilled  Promotional Review Specialist  to join their team for a 6+ Month engagement. This project involves review of promotional and educational material for medical and clinical accuracy. This is a high-impact role that requires a self-motivated professional who can hit the ground running and deliver results quickly.

Key Responsibilities & Deliverables:

This role is focused on the successful completion of specific tasks and deliverables. Your responsibilities will include:
  • Collaboration with teams:  Working with marketing to ensure promotional content is clinically accurate.
  • Review of Promotional Materials:  Review of promotional materials in the aprimo system to ensure medical and clinical accuracy and compliance.
  • Compliance Feedback:  Providing clear, concise, and compliant feedback to content owners to facilitate final material approval.
  • Documentation & Audit-Readiness:  Maintaining meticulous records of all review activities, approvals, and associated documentation within the online review system.
  • Regulatory Adherence:  Staying current on US & EU Medical Device industry guidance and compliance requirements to ensure all reviews meet current regulatory standards.
Required Skills & Experience:

We are looking for someone with a proven track record of successful contract engagements. The ideal candidate will have:
  • 3+ years of experience reviewing medical and clinical data for promotional purposes.
  • Deep expertise in the US & EU Medical Device industry, the promotional review process, and relevant guidance/compliance requirements. Strong understanding of clinical data is essential. This isn't a learning role—you need to be a subject matter expert.
  • Demonstrated ability to work autonomously and manage your own time effectively to meet project goals.
  • Experience with online review systems (such as aprimo) and regulatory compliance documentation. Familiarity with products in the Urology Space is a plus.
  • Strong communication skills to provide clear and concise status updates to the project team.

DeWinter Group and Maris Consulting  is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We post pay scales which are based on our client pay ranges. DeWinter, Maris, and our clients have the right to modify the requirements of the role which can impact the pay ranges posted.

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