The Data Coordinator provides support to Study Coordinator on a daily basis, ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines. You will support the Study Coordinator to meet industry trial data deadlines. You will obtain source documentation for patients enrolled into clinical trial. You will assist the Study Coordinator with case report form completion and query resolution. You will assist in Serious Adverse Event (SAE) reporting and tracking. You will create and maintain patient visit tracking spreadsheets for the Study Coordinator. You will maintain and archive study administrative files. You will be assigned special procedural projects to enhance the functioning of Drug Development Data Operations. Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.
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Job Type
Full-time
Career Level
Entry Level