About this opportunity
Vita Global Sciences, a Kelly Company lists this Global Medical Reviewer opportunity in city of rochester, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Kelly Science and Clinical FSP is currently seeking a Global Medical Reviewer for a long‑term engagement with one of our Global MedTech clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full‑time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
The Global Medical Reviewer will serve as the Medical Affairs reviewer for promotional and non‑promotional materials, ensuring that communications are scientifically accurate, evidence‑based, medically appropriate, and compliant with applicable regulations, approved labeling, and company policies.
This role works closely with Medical Affairs, Marketing, Regulatory Affairs, Legal, and Compliance teams to provide medical review and scientific guidance for a broad range of commercial and educational materials supporting our clients portfolio of energy‑based aesthetic technologies.
Scope of Work
Serve as the Medical Affairs reviewer within PRC/MLR review processes.
Review promotional, educational, scientific, and training materials for medical and scientific accuracy.
Ensure claims are appropriately supported by clinical evidence, published literature, approved labeling, and regulatory clearances.
Evaluate materials for balance, appropriate risk communication, and consistency with company standards.
Participate in review meetings and provide medical feedback regarding scientific claims and messaging.
Review materials intended for healthcare professionals, consumers, sales representatives, distributors, and internal stakeholders.
Support review activities across multiple global regions, including the United States, Canada, EMEA, and LATAM.
Scientific Review & Medical Guidance
Provide scientific interpretation of clinical data and published literature.
Support development and refinement of evidence‑based claims and scientific messaging.
Assist internal stakeholders with scientific and medical questions related to promotional materials.
Ensure consistency of scientific communication across products and regions.
Systems & Documentation
Review materials within Veeva PromoMats and associated review platforms.
Document review comments and approval decisions in accordance with company procedures.
Support inspection and audit readiness activities as required.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.