Medical Content and Review Specialist | 2–5 Years Experience | Salary: 6–10 LPA
Job Description
EVERSANA is seeking a Medical Content and Review Specialist to join its Clinical & Medical team in Pune, Maharashtra. This role is responsible for managing the Medical, Legal, and Regulatory (MLR) review process for pharmaceutical and healthcare clients, ensuring that all promotional and non-promotional content is accurate, compliant, and approved according to regulatory and organizational standards. The position also supports medical content development, project management activities, and Medical Affairs initiatives.
Key Responsibilities
Medical, Legal & Regulatory (MLR) Review Management
Manage the complete end-to-end MLR review process for assigned clients.
Schedule, organize, and lead Review Committee meetings.
Document live discussions and reviewer comments within Veeva Vault.
Prepare, circulate, finalize, and archive meeting minutes.
Ensure all communication materials are reviewed and approved through established MLR workflows.
Verify that submissions follow the correct review path and compliance requirements.
Reject incomplete or non-review-ready submissions.
Facilitate discussions during review meetings and maintain proper documentation.
Perform quality control checks between approved and final published documents.
Support FDA 2253 submission activities in collaboration with regulatory reviewers.
Medical Content Support
Assist in developing project plans for medical content initiatives.
Support medical writing and content development teams.
Upload and manage materials within client review and approval platforms.
Assist with document annotation, reference linking, and content preparation activities.
Medical Affairs & Project Management Support
Support Medical Affairs and Medical Information teams in managing strategic projects.
Monitor project timelines and deliverables to ensure successful execution.
Coordinate with cross-functional teams to maintain project progress and compliance.
Required Qualifications
Graduate degree in Life Sciences, Biomedical Sciences, Pharmacy, Biotechnology, or a related field.
Minimum 2 years of experience in a pharmaceutical company, healthcare agency, or life sciences organization.
Experience in Scientific Writing, Scientific Review, or MLR review processes.
Required Skills
Strong understanding of Medical, Legal, and Regulatory (MLR) review processes.
Hands-on experience with Veeva Vault PromoMats and/or Veeva Vault MedComms.
Excellent written and verbal communication skills in English.
Strong project management, organizational, and time management abilities.
Experience in meeting planning, coordination, and documentation.
Excellent attention to detail and quality control skills.
Strong customer service and stakeholder management capabilities.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
Ability to manage multiple projects and deadlines effectively.
Understanding of pharmaceutical compliance, medical communications, and healthcare regulations.
Uttar Pradesh :
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