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Senior Clinical Programmer

Senior Clinical Programmer

NOVARTIS

5 - 7 years

14 - 16 Lacs

Hyderabad

Posted:1 day ago| Platform:

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Skills Required

SAS Database design Functional testing Business analytics Analytical Clinical trials PLSQL Business intelligence Monitoring Python

Work Mode

Work from Office

Job Type

Full Time

Job Description

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.

About the Role

Major accountabilities:

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

Key performance indicators:

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

Minimum Requirements:
Work Experience:

At least 5-7 years 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:
Strong knowledge of programming languages (SQL, PL/SQL, C#, VB script, SAS, Python, R)
Strong knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview)
Knowledge of clinical data management systems and/or relational databases (e. g. OC/RDC, INFORM, RAVE) as applied to clinical trials
Attention to detail, quality, time management and customer focus
Ability to translate technical concepts for nontechnical users in the areas of clinical database design and data review reporting development
Strong verbal and written communication skills to work with our global partners and customers
Understanding of Drug Development Process, ICHGCP, CDISC standards and Health Authority guidelines and regulations
Ability to train and supervise new or less experienced associates.

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NOVARTIS

Pharmaceutical Manufacturing

Basel Baselstadt

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Senior Clinical Programmer