IQVIA
Healthcare
RaveCustomFunctionProgrammer
Neural analysis suggests this role is
optimal for Senior candidates.
“Rave Custom Function Programmer at IQVIA. Skills: RAVE, Clinical database programming, Global Library maintenance. Plan database design. Coordinate database design”
Industry & Context.
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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