Medical Content and Review Specialist job opportunity at EVERSANA.



Date2026-04-07T06:43:51.723Z bot
EVERSANA Medical Content and Review Specialist
Experience: General
Pattern: Full-time
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeGeneral
loacation Pune, Maharashtra, India
loacation Pune, Maharash..........India
Auto GPT Summarize Enabled

Job Description THE POSITION: The Medical, Legal and Regulatory (MLR) review is an essential process in healthcare marketing to make sure advertising, promotional and non-promotional content is accurate, compliant, and ready to be published. The MLR process must rigorously control and execute review, approval and document filing actions. As part of the MLR team, the Medical Content and Review Specialist is responsible for managing all the MLR process for a dedicated client. The Medical Content and Review Specialist ensures that all administrative and program management support for the client’s MLR process operates effectively and in full compliance with all internal and external policies and regulations.  ESSENTIAL DUTIES AND RESPONSIBILITIES: Our employees are tasked with delivering excellent business results through the efforts of their teams.  These results are achieved by:    MEDICAL CONTENT AND REVIEW SPECIALIST RESPONSIBILITIESManages the end-to-end MLR process.Responsible for scheduling, setting the agenda, and leading Review Committee meetings.Add live discussion notes for comments discussed in Veeva VaultScribe meeting minutes, circulate draft meeting minutes for Committee approval and finalizeand file approved minutesEnsure all covered communications are properly vetted through the review process utilizing the online review system (e.g., Veeva Vault PromoMats and Vault MedComms)Cascade and enforce any new policies and guidelines related to review of materials.Verifies that materials are assigned to the appropriate review pathRejects incomplete submissions and materials that are not review readyFacilitates/documents discussion in live meetings.QCs Final Document vs. Approved DocumentSupports FDA 2253 submissions with MLR Regulatory Reviewer/Partner MEDICAL CONTENT SUPPORT RESPONSIBILITIESSupport the development of project plansSupport medical content development teamSupport upload of materials into clients’ review and approval platforms, including supporting annotating, anchoring references, etc. MEDICAL AFFAIRS AND MEDICAL INFORMATION PROJECT MANAGEMENT SUPPORTSupport Medical Affairs and Medical Information leadership in developing and managing project plans for key initiatives All other duties as assigned.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

Other Ai Matches

Transportation Coordinator (2nd shift) Applicants are expected to have a solid experience in handling Job related tasks
Medical Science Liaison Applicants are expected to have a solid experience in handling Job related tasks
Group Copy Supervisor (must have pharma agency exp) Applicants are expected to have a solid experience in handling Job related tasks
Marketing Manager II (Account/Project Management) Applicants are expected to have a solid experience in handling Job related tasks