Medical Information Specialist

Tata Consultancy Services · Maharashtra, India

TCS is hiring for Life Sciences Medical Information Manager: Medical Information

Job Location: Hyderabad, Mumbai, Bangalore, Noida

Experience Range: 4 to 8 years

Educational Qualification(s) Required:

• Bachelor's degree in Life Sciences, Pharmacy, Medicine, Nursing, or related healthcare field

• Advanced degree (PharmD, PhD, MD) preferred

Technical/Domain Skills:

Medical Enquiry Response Development

• This role is responsible for Conducting Scientific literature reviews and synthesize information to support the development of medical enquiries/frequently asked questions (FAQs).
• Lead the authoring, review, and approval of medical enquiry responses, including:
• Standard Response Documents (SRDs)
• Customized responses to unsolicited enquiries
• Frequently Asked Questions (FAQs)
• Off label and complex enquiry response development
• Ensure enquiry responses are non promotional, evidence based, and scientifically accurate.
• Perform and oversee targeted literature searches, data interpretation, and reference management.
• Ensure compliance with global and local regulations, company SOPs, and Medical Affairs governance.
• Support medical review (MLR) processes for enquiry responses.

Scientific Content Strategy & Knowledge Management

• Own and maintain the medical enquiry responses (content) library, ensuring version control and periodic updates.
• Monitor label updates, clinical data changes, and safety information to trigger response revisions.

Other Responsibilities: -

• Review and quality check enquiry responses for scientific rigor, clarity, and compliance.
• Contribute to process improvement, automation initiatives, and audit readiness.
• 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.
• Knowledge and application of good practices in medical enquiry management and writing for Medical Information.
• 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.
• Fluency in oral and written English.
• Experience with various therapeutic areas.
• Solid understanding of medical concepts and the implications on a broader scale in the pharmaceutical industry (regulatory, PV, legal, commercial, drug development, etc).

Regards

Manisha Singh (TCS HR)