REQ-10078751
May 26, 2026
LOC_IN
About the Role
Major accountabilities:
- Provide timely and quality responses to medical enquiries escalated from Novartis country affiliates for products
- Write MI deliverables such as Global Guidance Documents (GGDs), MI Q&As to ensure they meet quality requirements – scientifically balanced and evidence-based, adhere to topic, using appropriate language and correct grammar, and regulatory/safety/legal aspects are considered
- Provide input into MI processes and standards to ensure optimal efficiency and productivity
Essential Requirements:
- Healthcare professional degree or degree in a healthcare-related field. Advanced degree (PhD, PharmD, MD) in life science/healthcare
- Minimum 2 years’ experience in a Medical Information/Communications role specifically in the Pharmaceutical Industry (or a related Medical Affairs role with significant MI responsibility in the Pharmaceutical Industry)
- Experience with delivering MI services at Global and local level
- Product and disease area knowledge in Novartis therapeutic areas
- Strong knowledge of good practices in medical information writing, and experience with mentoring others
- Strong clients focus and cross-functional skills and proven experience in collaboration with other departments/groups
Skills Desired
Clinical Research, Clinical Trials, Detail-Oriented, Medical Writing, Safety
Role Requirements
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
DIV_GD
Development
LOC_IN
Hyderabad (Office)
IN10 (FCRS = IN010) Novartis Healthcare Private Limited
FCT_RD
Full time
Regular
No