Associate Clinical Programmer

Job Description Summary

Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, reports development, coordinate validation and rollout activities along with providing quantitative analytical support. These tasks are to be performed team based with general direction and supervision.

 

Job Description

Major Activities (Describe 8-12 main activities)

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. To provide quantitative analytical support to the global program teams, including providing support on analyzing reports

4. 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 making

6. Create, file and maintain appropriate documentation

7. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data

8. Program reports of low to medium complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R

9. Basic understanding of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output

 

Skills Desired

Clinical Trials, Computer Programming, Data Analysis, Programming Languages