REQ-10091059
Oct 30, 2026
LOC_IN
About the Role
Key Responsibilities
- Act as the primary interface between cross functional stakeholders, biostatisticians, statistical programmers, and technical teams.
- Lead requirement gathering workshops and support translating clinical/statistical needs into structured functional and technical specifications.
- Manage small team with oversight on their work deliverables ensuring productive outcomes.
- Oversee design and delivery of key releases and ensure end-to-end requirement traceability across development, validation, and deployment phases.
- Ensure regulatory compliance, audit readiness, and adherence to documentation and governance standards.
Essential Requirements
- 12-14 years of experience in analytics, statistical programming, or software development. Proven experience in pharmaceutical or clinical research domain engagements with good understanding of clinical trial lifecycle
- Knowledge of emerging Technologies/Technology platforms and Operations.
- Team Management experience
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
LOC_GB
FCT_RD
Full time
Regular
No
