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Clinical Programmer

Clinical Programmer

NOVARTIS

2 - 5 years

9 - 10 Lacs

Mumbai

Posted:1 day ago| Platform:

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Skills Required

Statistical programming SAS Database design Business analytics Analytical Clinical trials PLSQL Business intelligence Monitoring Python

Work Mode

Work from Office

Job Type

Full Time

Job Description

Summary

-Responsible to support all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities.

About the Role

Major accountabilities:

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. Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery
4. To provide quantitative analytical support to the global program teams, including providing support on analyzing reports
5. Support the planning, execution and close-out of Clinical Programs/Trials.
6. Support the management in collation and delivery of analytics reports for critical decision making
7. Create, file and maintain appropriate documentation
8. Work with the internal SMEs and key stakeholders in providing analysis and interpretation of clinical program/trial operational data
9. Provide necessary training to end-user on best / appropriate and consistent use of various data review tools
10. Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, C#, VB script, SAS, Python, R
11. Good understanding of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output

Key performance indicators:

A Quality and timeliness of deliverables
2. Revisions to deliverables caused by logic or programming errors
3. Customer feedback and satisfaction

Minimum Requirements:
Work Experience:

2-5 years of experience in clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry as well as the following:
2. Strong knowledge of programming languages (SQL, PL/SQL, C#, VB script, SAS, Python, R)
3. Knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)
4. Understanding of clinical data management systems and/or relational databases as applied to clinical trials
5. Attention to detail, quality, time management and customer focus
6. Ability to translate technical concepts for nontechnical users in the areas of clinical database design and data review reporting development
7. Strong verbal and written communication skills to work with our global partners and customers
8. Understanding of Drug Development Process, ICHGCP, CDISC standards and Health Authority guidelines and regulation

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