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Medical Content And Review Specialist

Eversana
EVERSANA
Fresher years
3-5 LPA
Remote, India, India
10 April 27, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, Communication Skills, GCP guidelines, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Terminology, Narrative Writing, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Content and Review Specialist – MLR (Medical, Legal, Regulatory)


Location: Pune, Maharashtra, India
Job Type: Full-Time
Department: Clinical & Medical
Job Family: Medical Writing
Company: EVERSANA
Experience Required: Freshers or Minimum 2 years (suitable for freshers)


About the Company
EVERSANA is a globally recognized life sciences services organization dedicated to creating a healthier world. With a workforce of 7,000+ professionals and a client base of 650+ organizations ranging from biotech startups to leading pharmaceutical companies, EVERSANA delivers next-generation commercialization and medical solutions across the healthcare ecosystem.

The organization fosters a culture of inclusion, innovation, and patient-centricity, making it a preferred employer in the global pharmaceutical and healthcare industry.


Job Overview
The Medical Content and Review Specialist plays a critical role in managing the end-to-end Medical, Legal, and Regulatory (MLR) review process. This position ensures that all promotional and non-promotional healthcare content is scientifically accurate, compliant with global regulatory standards, and approved for publication.

This role requires strong coordination, scientific understanding, and expertise in medical review systems to support high-quality healthcare communications.


Key Responsibilities

MLR Process Management

  • Manage the complete lifecycle of the MLR review process for assigned clients

  • Schedule, organize, and lead MLR review committee meetings

  • Document live discussions, capture key review comments, and maintain meeting minutes

  • Ensure accurate documentation, approval tracking, and final archival of MLR records

  • Review and validate content submissions for completeness and compliance readiness

  • Assign materials to appropriate review workflows within Veeva Vault systems

  • Perform quality checks between final and approved documents

  • Support regulatory submissions including FDA Form 2253 processes

Medical Content Support

  • Assist in developing project plans for medical content initiatives

  • Support scientific content creation, annotation, and referencing

  • Upload and manage content within review platforms such as Veeva Vault PromoMats and MedComms

Medical Affairs & Project Management Support

  • Collaborate with Medical Affairs and Medical Information teams

  • Support execution and tracking of key medical projects and initiatives

  • Ensure adherence to timelines, quality standards, and regulatory requirements


Required Qualifications

Education

  • Bachelor’s or Master’s degree in Life Sciences, Biomedical Sciences, Pharmacy, or related field

Experience

  • Minimum 2 years of experience in a pharmaceutical company, CRO, or healthcare agency

  • Hands-on experience with Veeva Vault PromoMats and/or MedComms

  • Prior exposure to MLR review processes, scientific writing, or medical content review

Skills and Competencies

  • Strong understanding of MLR workflows, compliance, and regulatory frameworks

  • Excellent written and verbal communication skills in English

  • Strong project management, time management, and meeting coordination abilities

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)

  • High attention to detail and quality control


Why This Role Matters
This role sits at the intersection of medical science, regulatory compliance, and healthcare communication. It ensures that all healthcare-related content reaching patients and professionals is accurate, ethical, and compliant—directly contributing to patient safety and informed decision-making.


Important Note for Applicants
This is a mid-level role requiring prior experience in MLR review, medical writing, or scientific content management. Freshers are advised to begin with entry-level roles such as Medical Writer, Drug Safety Associate, or Clinical Data Associate before progressing into specialized MLR roles.


Equal Opportunity and Compliance Statement
EVERSANA is an Equal Opportunity Employer committed to diversity, equity, and inclusion. All qualified applicants will receive consideration without regard to race, gender, disability, or other protected characteristics.

The company maintains strict policies against recruitment fraud and does not request any payment or sensitive personal information during the hiring process.


How to Apply
Apply through the official careers page of the company or explore verified global pharmaceutical job opportunities on ThePharmaDaily.com.