Assistant Clinical Research Coordinator - (Richmond, VA)

The clinical research associate will perform all assigned roles in compliance with Good Clinical Practice and HIPPA and under the auspices of a Principal Investigator (PI). The incumbent will conduct all activities included under the PI’s delegation log including: study finding activities. These may include database searches, contact with sponsor’s and CRO’s. The incumbent may submit documents to IRB after completing appropriate training, and prepare and collect prescreening logs, screening logs, enrollment logs, informed consent checklists, eligibility checklists, serious adverse event reporting process and logs and collaborate with the PI to ensure and verify all documentation is complete. The incumbent will also be responsible for reviewing and abstracting data from CERNER, and ensuring all HIPPA identifiers are redacted prior to sending info to the sponsor.