Non-Clinical Medical Job at Tata Consultancy Services | Medical Information Job Opportunity!

Tata Consultancy Services (TCS) is a leading global IT services, consulting, and business solutions organization. Operating in various sectors, including Life Sciences, TCS is dedicated to delivering innovative solutions that drive business success.

Location: Mumbai Metropolitan Region
Experience Required: 4 to 8 years

Requirements

• Bachelor’s degree in Medicine or a related healthcare field
• Advanced degree (PharmD, PhD, MD) preferred
• Fluency in oral and written English
• Experience with various therapeutic areas
• Solid understanding of medical concepts and their implications in the pharmaceutical industry (regulatory, pharmacovigilance, legal, commercial, drug development, etc.)

Responsibilities

Medical Enquiry Response Development

• Conduct 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

Additional Responsibilities

• Review and quality-check enquiry responses for scientific rigor, clarity, and compliance
• Contribute to process improvement, automation initiatives, and audit readiness
• Ensure responses are scientifically balanced, evidence-based, adhere to key messages, and consider regulatory/safety/legal aspects
• Apply good practices in medical enquiry management and writing for Medical Information
• Collaborate with cross-functional teams (e.g., Clinical Development, Regulatory Affairs) and demonstrate strong interpersonal communication and presentation skills