Promotional Review and Production Specialist
Core
Prepare and manage Medical, Legal, and Regulatory (MLR) submission packages for biopharmaceutical promotional materials, ensuring accuracy and compliance before print production.
Role type
Senior IC regulatory and production specialist
Builds
MLR-approved promotional materials for print distribution
Domain
Biopharmaceuticals / Regulatory Affairs / Print Production
Required skills
Veeva RAPID, Veeva PromoMats, Veeva MedProduction, proofreading, reference management, claim-to-source linking, quality assurance checks, version control, deadline management
Preferred skills
Medical editing, scientific content review, promotional print production experience
Technologies
Veeva RAPID, Veeva PromoMats, Veeva MedProduction
Responsibilities
Prepare complete submission packages with supporting documentation; Upload and organize references, link claims to source passages; Perform quality assurance checks on final production files against approved content; Coordinate corrections with internal teams and production partners; Complete production approval and release steps; Maintain submission status and communicate risks to deadlines
Seniority
Senior, hands-on IC