Job Description Summary
Participate in the full lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support. These tasks are to be performed independently or team based with minimal guidance and supervision.
Job Description
1. Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data
2. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders
3. Author /co-author the user requirements document, functional specifications and functional testing scripts
4. Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery.
5. To provide quantitative analytical support to the global program teams, including providing support on analyzing reports
6. Support the planning, execution and close-out of Clinical Programs/Trials.
7. Support the management in collation and delivery of analytics reports for critical decision making
8. Create, file and maintain appropriate documentation
9. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data
10. Provide necessary training to end-user on best / appropriate and consistent use of various data review tools
11. Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R.
12. Good Knowledge of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output
13. Support special projects of limited scope (sub team lead, local project, etc.) both clinical and non-clinical in nature.
14. Provide study level expertise and involvement in CTTs.
15. Lead or provide support to special projects both clinical and non-clinical in nature or in general areas spanning various responsibilities but not limited to systems issues, processes, user support, training, etc.
Skills Desired
Clinical Trials, Computer Programming, Data Analysis, Programming Languages, Reporting, Statistical Analysis
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