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

Are you passionate about leveraging your expertise in life sciences to make a significant impact in the healthcare sector? Tata Consultancy Services (TCS) is seeking a dedicated Medical Information Specialist to join their innovative team in Mumbai. This Non-Clinical Medical Job in Mumbai offers a unique opportunity to work in a non-clinical medical setting, focusing on developing and managing medical enquiry responses.

With a commitment to excellence and a collaborative work environment, TCS is the perfect place for professionals eager to advance their careers in a global IT and consulting leader.

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. With a strong presence in Mumbai, TCS is committed to fostering a culture of excellence and continuous improvement, making it an ideal workplace for professionals seeking a non-clinical medical job.

• Position:
  Medical Information Specialist
• Location:
  
  Mumbai Metropolitan Region
• Experience
  
  Required:
  
  4 to 8 years

• Bachelor's degree in Medicine or a related healthcare field
• Advanced degree (PharmD, PhD, MD) preferred

• Medical Enquiry Response Development
• This role is responsible for conducting scientific literature reviews and synthesizing 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.

• 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.

• 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 (e.g., Clinical Development, Regulatory Affairs) and excellent interpersonal communication and presentation skills.
• Fluency in oral and written English.
• Experience with various therapeutic areas.
• Solid understanding of medical concepts and their implications on a broader scale in the pharmaceutical industry (regulatory, PV, legal, commercial, drug development, etc).