Medical Content And Review Specialist

Eversana

2+ years

Not Disclosed

Pune, Pune city, India

Openings: 10 June 10, 2026

Job Description

Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.

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Medical Content And Review Specialist

Job Description

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