Posted 19 August, 2026
Medical Information Specialist
Tata Consultancy Services
Mumbai, MH, IN
Full Time
Reference: 0ad0c92da590afaa
Job Description
TCS is hiring for Life Sciences Medical Information Manager: Medical Information
\nJob Location: Hyderabad, Mumbai, Bangalore, Noida
\nExperience Range: 4 to 8 years
\nEducational Qualification(s) Required:
\n• Bachelor's degree in Life Sciences, Pharmacy, Medicine, Nursing, or related healthcare field
\n• Advanced degree (PharmD, PhD, MD) preferred
\nTechnical/Domain Skills:
\nMedical Enquiry Response Development
\n- \n
- This role is responsible for Conducting Scientific literature reviews and synthesize information to support the development of medical enquiries/frequently asked questions (FAQs). \n
- Lead the authoring, review, and approval of medical enquiry responses, including: \n
- Standard Response Documents (SRDs) \n
- Customized responses to unsolicited enquiries \n
- Frequently Asked Questions (FAQs) \n
- Off‐label and complex enquiry response development \n
- Ensure enquiry responses are non‐promotional, evidence‐based, and scientifically accurate. \n
- Perform and oversee targeted literature searches, data interpretation, and reference management. \n
- Ensure compliance with global and local regulations, company SOPs, and Medical Affairs governance. \n
- Support medical review (MLR) processes for enquiry responses. \n
Scientific Content Strategy & Knowledge Management
\n- \n
- Own and maintain the medical enquiry responses (content) library, ensuring version control and periodic updates. \n
- Monitor label updates, clinical data changes, and safety information to trigger response revisions. \n
Other Responsibilities: -
\n- \n
- Review and quality‐check enquiry responses for scientific rigor, clarity, and compliance. \n
- Contribute to process improvement, automation initiatives, and audit readiness. \n
- Ensure the responses prepared are scientifically balanced and evidence-based, adhere to topic/key messages, language and grammar are correct, regulatory/safety/legal aspects are considered. \n
- Knowledge and application of good practices in medical enquiry management and writing for Medical Information. \n
- Strong cross-functional skills and proven experience in collaboration with other departments/groups (eg Clinical Development, Regulatory Affairs) and excellent interpersonal communication and presentations skills. \n
- Fluency in oral and written English. \n
- Experience with various therapeutic areas. \n
- Solid understanding of medical concepts and the implications on a broader scale in the pharmaceutical industry (regulatory, PV, legal, commercial, drug development, etc). \n
Regards
\nManisha Singh (TCS HR)