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Clinical Data Coordinator Jobs
Company | Medix™ |
Address | Pennsylvania, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-09-22 |
Posted at | 8 months ago |
FULLY REMOTE | CLINICAL DATA COORDINATOR | EAST COAST | APPLY TODAY
Job Summary
Under the direction of the Clinical Research Manager, the research associate will work with physicians, nurses and allied health professionals to facilitate clinical research trials and independently execute job functions related to protocol management.
Duties and Responsibilities
- Assists the research team with the screening process and ensures that subject’s records, archival tissue, radiology tests, lab work results, etc. are obtained prior to subject entry into a study.
- Assists with monitoring visits and coordinate data collection including data locks.
- Assists in the consent process for patients on minimal risk/non-therapeutic trials.
- Responsible for lab kit inventory, preparation and tissue requests.
- Responsible for prompt and accurate data entry for protocols, including Serious Adverse Events.
- Performs query resolution.
- Performs study specified electrocardiograms.
- Works with research team in managing the visits of active and follow up subjects on research protocols.
- Attends study related biopsies and transports tissue samples for processing.
- Assists in the coordination of initiation, site evaluation, monitoring visits, and audits required by the sponsor.
- Maintains patient tracking spreadsheets to ensure data entry requirements are met.
- Demonstrates industry accepted good documentation and clinical practices during the conduct of research to collect quality data, in compliance with institutional, and statutory guidelines.
- Processes study specific data collection documents into case report forms.
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