Description
The role supports clinical trial data management by developing and maintaining EDC databases, creating CRF annotations and mapping specifications, importing and transforming datasets, performing data cleaning and reconciliation, and producing regular or ad-hoc reports. Responsibilities include database design, EDC edit programming, listings, scheduled reports, and use of tools such as Medidata Rave, Oracle Inform, Cognos, Business Objects, R, and Spotfire, while following GCP and computerized-systems-compliance requirements.
