Data Coordinator

Prepares documentation, such as CCGs, Data Management Plan (DMP), Data Report Specifications, External Data Transfer Specifications, etc.
Assists in developing standard test data for testing screens and listings and provides feedback on the results of the testing
Performs user acceptance testing on studies, including testing of edit checks, etc.
Assists in maintaining DBs and supports DB updates Tracks CRFs
Performs data entry
Generates reports for data review
Reviews CRFs, data listings to ensure all data captured follow protocol, CCGs, DMP, etc.
Reviews responses to queries and resolves discrepancies
Performs external data reconciliation
Acts as a Lead Data Coordinator on multiple studies
Performs document submission to Trial Master File (TMF)
Supports TMF Quality Control (QC) activities
Performs database QC activities
Performs QC of study reports, CRF archive files
Supports the Data Scientist and/or PM in reporting financial project stats, study metrics, dashboard updates, project status

What we are searching for:

Typically requires 2 -4 years of DM mastery or related clinical research industry experience
Knowledge of at least one Clinical Data Management System (CDMS) (e.g. Madidate Rave,DataLabs EDC, etc.).

Clinical Trial Administrator