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.
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