Clinical Research Data Coordinator
By Sarah Cannon At Girlstown USA, TX, United States
Experience using EMR and strong computer skills preferred.
You will maintain working knowledge of protocols and eCRF completion guidelines for assigned projects.
You will regularly review protocol, amendments or clarifications, and revisions for eDC data entry.
You will support non-treatment studies. You will abstract and analyze data from necessary sources to complete the EDC and resolve queries.
A strong understanding of research protocols and implementation.
Attention to details and accuracy