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. This role is responsible for managing the Medical, Legal, and Regulatory (MLR) review process for dedicated pharmaceutical and healthcare clients. The position ensures that promotional and non-promotional healthcare content is reviewed, approved, documented, and published in compliance with internal policies, industry regulations, and regulatory requirements.

The ideal candidate will have experience in scientific writing, medical review, regulatory compliance, and project management within the pharmaceutical, healthcare, or life sciences industry.

Key Responsibilities

MLR Review Process Management

Manage the end-to-end Medical, Legal, and Regulatory (MLR) review process.
Schedule, organize, and lead Review Committee meetings.
Document live discussions and comments within Veeva Vault.
Prepare, circulate, finalize, and archive meeting minutes.
Ensure all communication materials undergo proper review and approval procedures.
Verify that submissions follow the appropriate review workflow.
Reject incomplete or non-review-ready materials.
Facilitate and document discussions during review meetings.
Conduct quality checks on final documents against approved versions.
Support FDA 2253 submission activities alongside regulatory reviewers.

Medical Content Support

Assist in developing project plans for medical content initiatives.
Support medical content development teams throughout project execution.
Upload and manage content within review and approval platforms.
Support annotation, reference anchoring, and content preparation activities.

Medical Affairs & Project Management Support

Assist Medical Affairs and Medical Information teams in planning and executing strategic projects.
Monitor project timelines and deliverables.
Support cross-functional collaboration and communication among stakeholders.

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 and organizational skills.
Effective meeting planning and coordination abilities.
Excellent attention to detail and documentation skills.
Strong stakeholder management and customer service orientation.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
Ability to manage multiple projects and deadlines simultaneously.
Knowledge of pharmaceutical compliance and healthcare regulations.

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Medical Content And Review Specialist

Job Description

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