Your responsibilities include, but are not limited to:

•Contribute to electronic Case Report Form (eCRF) development with a thorough understanding of data to be collected and in alignment with the protocol.

•Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards (for CRFs as well as 3rd party data collection methodologies) for assigned trials/therapy areas as needed.

•Provide timely information for, and support the setup and finalization of, accurate and high-quality Data Transfer Specification (DTS) documents.

•Help define a timely transfer schedule for rapid data availability and review. Act as facilitator / problem solver between all parties involved (e.g., clinical functions, data operations, vendors) to streamline and accelerate DTS finalization and revision.

•Provide expert input into the Data Quality Plan (DQP) with a f...