27 dagen geleden
Support and drive the data management process within the organization to meet internal and client deadlines.
Design and build the CRF/eCRF.
Write the Data Management Plan for studies and to update as necessary throughout the duration of studies.
To carry out regular checks, and program in additional checks, to validate and verify information held in the study databases in accordance with the validation checks detailed in the data management plan.
Raise and resolve data queries with Site Engagement Managers, study centres and CROs.
Point of contact for sites, clients and CROs and support the completion of CRFs.
Provide technical support to internal and external personnel in the use of the eDC system.
Educated to degree level (preferably Life Science).
Experience in Clinical Data Management.