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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