Clinical Programmer

Job description

Job Description

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, report programming, coordinate validation and rollout activities along with providing quantitative analytical support. These tasks are to be performed independently or team based with guidance and supervision.• 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 and monitoring of clinical data for key stakeholders • Facilitate interaction with end-user on creating specifications and working with programmers or performing the programming activities for successful delivery • To provide quantitative analytical support to the global program teams, including providing support on analyzing reports • Support the planning, execution and close-out of Clinical Programs/Trials. • Support the management in collation and delivery of analytics reports for critical decision making • Create, file and maintain appropriate documentation • Work with the internal SMEs and key stakeholders in providing analysis and 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 • Good understanding of Novartis Clinical Data Standards and its implementation for creation of reports specifications or reports output
Position Title

Clinical Programmer

Desired profile

Minimum requirements

University or college degree in Life Sciences, Mathematics, Computer Science, Medical Informatics or equivalent degree. Fluent English (oral and written). • 2-5 years of experience in clinical review and reporting pro-gramming, 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) • Knowledge of Data Review and/or Business Intelligence tools (such as Spotfire, JReview) • Understanding of clinical data management systems and/or relational databases as applied to clinical trials • Attention to detail, quality, time management and customer focus • Ability to translate technical concepts for non-technical 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, ICH-GCP, CDISC standards and Health Authority guidelines and regulations
Job Type

Full Time
Country

India
Work Location

Hyderabad
Functional Area

Research & Development
Division

Global Drug Development
Business Unit

GDO GDD
Employment Type

Regular
Company/Legal Entity

Nov Hltcr Shared Services Ind