Medical Writer Job at MSN Laboratories – Apply Now
Medical Writer Job: MSN Laboratories is inviting applications from qualified medical professionals for the position of Medical Writer – Medical Reviewer. This role is ideal for doctors looking to build or advance a career in pharmacovigilance and drug safety, with direct involvement in medical review, regulatory case assessment, and aggregate safety reporting. The opportunity offers exposure to global safety standards, regulatory documentation, and signal management activities within a reputed pharmaceutical organization.
Medical Writer Job Details
- Job Title: Medical Writer
- Job Function: Pharmacovigilance/Drug Safety
- Employment Type: Full-time
- Work Location: As per company requirements
About the Company
MSN Laboratories is a well-established pharmaceutical company known for its strong presence in research, development, manufacturing, and global regulatory compliance. The organization focuses on delivering high-quality, affordable medicines while maintaining stringent safety and compliance standards. MSN Laboratories offers a professional work environment that encourages scientific integrity, continuous learning, and career growth in core pharmaceutical domains such as pharmacovigilance and medical affairs.
Medical Writer Job: Qualifications
- MBBS or MD (Pharmacology)
- Strong medical knowledge with an understanding of adverse event reporting
- Familiarity with pharmacovigilance concepts and regulatory guidelines
- Ability to critically analyze clinical and safety data
About the Role
The Medical Writer – Medical Reviewer will be responsible for the medical review of individual case safety reports (ICSRs) from company sources, literature, and regulatory authorities. The role requires sound clinical judgment to assess adverse events, evaluate causality, and ensure high-quality medical documentation in compliance with global regulatory standards.
Key Responsibilities
- Medical review of the company, literature, and regulatory safety cases
- Selection and assessment of adverse events, including seriousness criteria
- Accurate MedDRA coding of adverse events
- Review of reporter and company causality and label assessment
- Identification of product role (suspect, concomitant, or interacting)
- Evaluation of case narratives, medical history, lab data, and concomitant conditions
- Drafting, quality check, and medical review of PSURs and PADERs
- Medical review of Risk Management Plans (RMPs)
- Review of Signal Management Reports
. MBBS or MD pharmacology professionals can apply.){kind=link}