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Clinical Research Coordinator
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- Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned.
- Understands and can conduct clinical research studies that require but not limited to, DSMB, Emergent Access, Conduct Investigator Initiated studies, Multi-site clinical trials, Research Team training manuals.
- Achieves clinical research coordinator certification from ACRP or SOCRA after two years in the position.
- Supporting NCCBD's NCORP: NCI Community Oncology Research Program across the Nemours enterprise.
- Participates in training nursing and ancillary study staff for study purposes; recruits, screens and enrolls sufficient number of study participants in conformance with protocol requirements.
Expired 11 days agoInactive Job
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