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Medical Content And Review Specialist

Eversana
EVERSANA
2+ years
Not Disclosed
Pune, India
10 May 18, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: 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

Company: EVERSANA
Location: Pune
Department: Clinical & Medical
Job Family: Medical Writing
Employment Type: Full-time


About EVERSANA

EVERSANA is a globally recognized healthcare commercialization company with over 7,000 employees supporting more than 650 pharmaceutical and biotech clients worldwide. The organization focuses on helping innovative therapies reach patients through next-generation commercialization services.

The company emphasizes:

  • Diversity, Equity & Inclusion (DE&I)

  • Patient-centered innovation

  • Collaborative work culture

  • Professional growth and development


Position Overview

The Medical Content and Review Specialist is part of the Medical, Legal, and Regulatory (MLR) review team. The role focuses on managing the complete MLR review process to ensure healthcare promotional and non-promotional materials are:

  • Accurate

  • Compliant

  • Properly reviewed

  • Approved for publication

The specialist acts as a key coordinator between stakeholders while ensuring adherence to internal and external regulatory standards.


Key Responsibilities

MLR Process Management

  • Manage the end-to-end Medical, Legal & Regulatory (MLR) review process

  • Schedule and lead Review Committee meetings

  • Prepare agendas for meetings

  • Document live meeting discussions in:

    • Veeva Vault PromoMats

    • Vault MedComms

Documentation & Compliance

  • Record and circulate meeting minutes

  • Finalize and archive approved meeting documentation

  • Ensure all communications undergo proper review workflows

  • Verify materials are assigned to appropriate review pathways

  • Reject incomplete or non-review-ready submissions

  • Support compliance with:

    • Internal policies

    • External regulations

    • FDA submission requirements (2253 submissions)

Quality Control

  • Conduct QC checks between:

    • Final documents

    • Approved documents

Medical Content Support

  • Assist medical content development teams

  • Support project plan creation

  • Upload and manage materials within review systems

  • Assist with:

    • Reference anchoring

    • Annotation

    • Content formatting

Project Management Support

  • Support Medical Affairs and Medical Information leadership

  • Help manage timelines and project execution for strategic initiatives

Additional Duties

  • Perform other assigned responsibilities as needed


Required Qualifications

Education

  • Graduate degree in:

    • Life Sciences

    • Biomedical Sciences

    • Related healthcare field

Experience

  • Minimum 2 years of experience in:

    • Pharmaceutical companies, or

    • Healthcare agencies

Required Skills & Expertise

  • Experience with:

    • Scientific writing

    • Scientific review

    • MLR review processes

  • Strong project management and time management skills

  • Meeting coordination and facilitation experience

  • Excellent customer service and communication abilities

Technical Skills

  • Experience with:

    • Veeva Vault PromoMats

    • Vault MedComms

  • Proficiency in:

    • Microsoft Outlook

    • Microsoft Word

    • Excel

    • PowerPoint

    • Windows applications

Communication Skills

  • Excellent English communication:

    • Written

    • Verbal


Work Environment & Culture

Diversity & Inclusion

EVERSANA promotes an inclusive workplace that values:

  • Diversity of backgrounds

  • Different perspectives

  • Equal opportunity employment

Professional Environment

  • Collaborative healthcare-focused culture

  • Opportunity to work with global pharmaceutical clients

  • Exposure to regulatory and medical communication processes


Important Candidate Information

EVERSANA warns candidates about fraudulent recruitment scams. The company:

  • Never requests payment during hiring

  • Never asks for sensitive personal information during recruitment

  • Encourages applicants to verify official communication channels


Ideal Candidate Profile

This role is well-suited for professionals who:

  • Have experience in MLR review or scientific writing

  • Enjoy coordination and compliance-focused work

  • Are detail-oriented and organized

  • Want exposure to pharmaceutical regulatory processes

  • Can manage multiple stakeholders and deadlines effectively