Develop and maintain trial specific Medidata Rave Databases, including eCRF’s, edit Checks and Custom
Functions using relevant programming languages (SQL, PL/SQL, C #), of various levels of complexity for
Phase I-IV with guidance.
Participates in study specific database set-up in Rave Application
Develop the eCRF layout and corresponding database according to documented trial specific
requirements using components from existing libraries.
Maintain and update the eCRF application and its components as required for protocol amendments
or required post production changes.
Develop departmental specifications and provide support for outsourced trials.
Create, file and maintain appropriate trial documentation.
Works closely with the testing group to ensure all programming issues are resolved in a timely manner
and study timelines are met.
Trouble-shoots and solves study build issues and programming issues with minimal guidance
Configures and programs additional system features, as required
Actively involved in Peer Reviewing the clinical programming activities.
Assist with in-progress audits as needed
To be successful in the role, you will have:
4-year Bachelor degree or local equivalent in Life Sciences, Mathematics, Computer Science, Medical
Informatics or equivalent degree
At least 3 years’ experience in clinical database programming, setup of clinical databases and CRF
design Edit Checks, CF and Migration, gained in the pharmaceutical industry, CRO or Life science related
industry as well as the following:
Strong knowledge of SQL, PL/SQL, C#
Knowledge of clinical data management systems and/or relational databases as applied to clinical
Location: Chennai/ Bangalore
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