Medical Content and Review Specialist – EVERSANA
Location: Pune, Maharashtra, India
Job Type: Full-Time
Department: Clinical & Medical
Job Category: Medical Writing | Medical Affairs | MLR Review | Scientific Content Management
About EVERSANA
EVERSANA is a globally recognized life sciences services organization dedicated to creating a healthier world through innovation, compliance excellence, and patient-focused healthcare solutions. With a workforce of 7,000+ professionals worldwide, EVERSANA partners with pharmaceutical companies, biotech firms, and healthcare organizations to deliver advanced commercialization and medical solutions across the healthcare industry.
Recognized as a Great Place to Work globally, EVERSANA fosters a collaborative, inclusive, and growth-driven environment for healthcare and life sciences professionals.
Job Title
Medical Content and Review Specialist
Job Location
Pune, Maharashtra, India
Employment Type
Full-Time
Experience Required
Minimum 2 Years of Experience Required
Freshers are not eligible for this role
Educational Qualification
Bachelor’s or Master’s Degree in:
Pharmacy
Life Sciences
Biomedical Sciences
Biotechnology
Clinical Research
Related Healthcare or Medical Fields
About the Role
EVERSANA is hiring an experienced Medical Content and Review Specialist to support Medical, Legal, and Regulatory (MLR) review operations for healthcare and pharmaceutical clients. The selected candidate will manage end-to-end MLR workflows, medical content coordination, scientific review documentation, compliance tracking, and project management activities.
This role is ideal for professionals with experience in:
Medical Writing
Scientific Review
MLR Operations
Veeva Vault PromoMats
Medical Affairs
Pharmaceutical Compliance
Regulatory Content Management
Candidates with strong communication skills, healthcare content review expertise, and pharmaceutical project management experience will be highly preferred.
Key Responsibilities
MLR Review & Compliance Management
Manage complete end-to-end Medical, Legal, and Regulatory (MLR) review processes
Schedule and coordinate Review Committee meetings
Prepare agendas and facilitate review discussions
Document live review comments within Veeva Vault systems
Prepare, circulate, finalize, and file meeting minutes
Ensure all promotional and non-promotional materials comply with regulatory standards
Verify proper review routing and workflow approvals
Reject incomplete or non-review-ready submissions
Conduct Quality Checks (QC) between approved and final documents
Support FDA 2253 submission activities alongside regulatory teams
Implement and enforce updated MLR review guidelines and policies
Medical Content Support
Assist medical content development teams
Support medical communication workflows
Upload and manage content in review platforms like:
Veeva Vault PromoMats
Vault MedComms
Support annotation and reference anchoring processes
Assist in project planning and documentation management
Medical Affairs & Project Management
Support Medical Affairs leadership in operational activities
Assist with project tracking and execution
Coordinate timelines and stakeholder communications
Support key strategic medical initiatives
Required Skills
Technical Skills
Veeva Vault PromoMats
Vault MedComms
Scientific Writing
Scientific Reviewing
Medical Content Management
Regulatory Documentation
MLR Review Process
Medical Affairs Operations
Pharmaceutical Compliance
Project Management
Soft Skills
Excellent English communication skills
Strong meeting coordination abilities
Time management and multitasking
Attention to detail
Customer service orientation
Documentation and reporting skills
Software & Tools
Candidates should have proficiency in:
Microsoft Outlook
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Windows-based applications
Veeva Vault Systems
Who Should Apply?
This opportunity is ideal for:
Medical Writers
MLR Review Professionals
Pharmacovigilance Professionals transitioning into Medical Affairs
Scientific Review Specialists
Medical Content Coordinators
Regulatory Affairs Professionals
Healthcare Project Coordinators
Professionals with prior pharmaceutical company or healthcare agency experience will have a strong advantage.
Why Join EVERSANA?
Global healthcare organization exposure
Career growth in Medical Affairs and Regulatory Operations
Opportunity to work with international pharmaceutical clients
Strong professional development culture
Inclusive and diverse workplace environment
Exposure to advanced healthcare commercialization systems
Important Note
EVERSANA does not charge any fee during recruitment, interview, or onboarding processes. Candidates are advised to apply only through official company career portals and verified recruitment channels.a
Apply Now
Explore more latest Pharmacovigilance, Medical Writing, Regulatory Affairs, Clinical Research, and Medical Affairs jobs globally on:
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