REQ-10075062
Apr 17, 2026
LOC_IN

About the Role

Major accountabilities:

  • 1. Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data2. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders3. To provide quantitative analytical support to the global program teams, including providing support on analyzing reports4. Support the planning, execution and close-out of Clinical Programs/Trials.5. Support the management in collation and delivery of analytics reports for critical decision making6. Create, file and maintain appropriate documentation7. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data8. Program reports of low to medium complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R9. Basic understanding of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output

Skills:

  • Clinical Trials.
  • Computer Programming.
  • Data Analysis.
  • Programming Languages.

Languages :

  • English.

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)
FCT_RD
Full time
Regular
No
careers default image
REQ-10075062

Associate Clinical Programmer

Apply to Job