IQVIA

Healthcare

RaveCustomFunctionProgrammer

₹19–28L ~AI est. Kolkata, West Bengal, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Rave Custom Function Programmer at IQVIA. Skills: RAVE, Clinical database programming, Global Library maintenance. Plan database design. Coordinate database design”

Industry & Context.

Healthcare
Problems you'll solve

Identifying and resolving issues

What They're Looking For.

Must Have

2 years clinical database programming, Setup of clinical databases, CRF design experience, RAVE certified, Global Library maintenance, Procedure building, Custom function programming, Basic CDISC Understanding

Nice to Have

Knowledge of Development of validation and derivation procedures, Scripting language experience

What You'll Do.

Coordinate database design

Develop database design

Implement database design

Maintain database design

Support database design

Maintain global libraries

Modify existing modules

Manage global library

Build global library objects

Maintain global library objects

Document global library objects

Facilitate creation of databases

Implement new library objects

Implement modified library objects

Understand data requirements

Support creation of metadata specifications

Contribute to review of SOPs

Provide input to SOPs

Document CDMS validations

Develop CDMS validations

Test CDMS validations

Maintain CDMS validations

Document CDMS derivations

Develop CDMS derivations

Test CDMS derivations

Maintain CDMS derivations

Discuss technical issues

Develop library objects

Document library objects

Review library copy groups

Maintain library copy groups

Consider maintenance of conventions document

How You'll Work.

Team & Collaboration

Working alongside Data Management; Work with other global librarians; Work with Data Managers; Work with Database Developers; Work with Data Standards Governance team; Work with metadata team

Communication Scope

Translate technical concepts

Full Job Description

Join global organization with 82000+ employees around the world, as Senior Database Management Specialist. You will be part of IQVIA’s world class technology team and will be involved in design, development, enhanced software programs, cloud applications, and proprietary products. **RESPONSIBILITIES** * Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems with guidance from senior staff. * Building new modules and maintaining global libraries for clinical trials. * Working alongside Data Management to modify existing modules & Management of a global library for a large number of projects. * Good Knowledge of Data Clinical Standards, Data Models and its implementation for database and GLIB development * Identifying and resolving issues which may negatively impact delivery of global library objects. Escalating issues to leadership as needed. * Building, maintaining and documenting the global library objects in order to facilitate the creation of Study Level databases to collect clinical trial data. * Working with the Data Managers – Study Start Up and Database Developers to implement new or modified global library objects. * Work with other global librarians (GL) to understand the data requirements for collection and submission under general supervision. * Support more experienced GL with the creation of metadata specifications that define the data content and structures for collection, transformation, and CDISC SDTM submission requirements, with general direction. * Contribute to the review of global SOPs and business guidance/user guides directly impacting the function and providing input when applicable. * Document, develop, test and maintain CDMS validations and derivations procedures using (SQL, PL/SQL, C #, VB script, SAS). * With general direction, work with the Data Standards Governance team, other GL’s and/or members of the metadata team to discuss technical issues with implementation of approved

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