Novartis Clinical Programmer Job

Novartis Clinical Programmer Job Opening For Life Sciences

Novartis Clinical Programmer Job Opening For Life Sciences. Life Science candidates apply online for a Senior Clinical Programmer position that is available at Novartis. Novartis is hiring msc candidates, as per the details below in their Research & Development area:

Job Title: Senior Clinical Programmer

Job ID: 302834BR

Location: Hyderabad, AP

Division: Global Drug Development

Business Unit: GDO GDD

Employment Type: Full-time

Job Description:

The number of projects that you would certainly lead or support across multiple therapeutic areas. We are looking for an experienced professional with robust programming competencies (SAS, SQL, Python, R, etc.) & strong communication abilities for our Clinical Database Development Reporting & Analytics function. As a member of this function, you would certainly be primarily responsible for seamless end to end data flow of Clinical & Operational Data from Data Collection, Transformation, Reporting & Analytics & provisioning of data to downstream applications & teams.

Your key responsibilities:

Your obligations consist of, however, are not limited to:

  • Produce and track reports for various line functions within Global Drug Development, used for ongoing monitoring of clinical data. Provide understandable and actionable reports on clinical data as well as monitoring of clinical data for key stakeholders
  • Author/ co-author the user requirements document, functional specifications and functional testing scripts
  • Facilitate interaction with end-user on creating specifications as well as working with programmers or performing the programming activities for successful delivery.
  • To provide quantitative analytical support to the global program teams, consisting of providing support on analyzing reports. Support the planning, execution and also close-out of Clinical Programs/Trials. Support the management in collation and delivery of analytics reports for critical decision making
  • Create, file and also maintain appropriate documentation. Work with the internal SMEs and also key stakeholders in providing analysis and also the interpretation of clinical program/trial operational data. Provide necessary training to end-user on best/ appropriate and consistent use of various data review tools
  • Program reports of various complexity from documented requirements, within the clinical reporting systems, using SQL, PL/SQL, C#, VB script, SAS, Python, R.
  • Excellent Knowledge of Novartis Clinical Data Standards and its implementation for the creation of reports specifications or reports output. Support special projects of limited scope (sub-team lead, local project, etc.) both clinical as well as non-clinical in nature.
  • Provide study level expertise and also involvement in CTTs. Lead or provide support to special projects both clinical and non-clinical in nature or in general areas spanning various responsibilities yet not limited to systems issues, procedures, user support, training, etc.

Minimum requirements:

  • University or college degree in Life Sciences or equivalent degree.
  • A minimum of 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 associated 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. Understanding of Drug
  • Development Process, ICH-GCP, CDISC standards as well as Health Authority guidelines as well as regulations.
  • Capability to translate technical concepts for non-technical users in the areas of clinical database design and data review reporting development.
  • Attention to detail, quality, time management and customer focus. Strong verbal and written communication abilities to work with our global partners and also customers.


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