Clinical Data Coordinator (North Comm Site) Cancer Center

Responsible for overall knowledge of protocols as assigned by the Director, Clinical Trials Office. Maintain screening/enrollment logs for each assigned protocol. Work collaboratively with the physician, nurse clinician, pharmacy and laboratory personnel to ensure tests/procedures/specimen collection, etc. are obtained per protocol. Communicate regarding patient data, status and protocol requirements with research staff. Conduct clinical trial in accordance with ICH/CFR/GCP and responsible for all data completion; query resolution for assigned protocols. Assist with the identification and reporting of Adverse and Serious Adverse events in accordance with ICH/CFR/GCP and specific protocol. Attend study specific training to include but not limited to Study Initiation and Internal Kick-off Meeting. Prepare and provide patient status report as requested by the Director, Clinical Trials Office. Research and resolve data discrepancies; coordinate final database closure activities and participate in customer audits and process improvement initiatives. 4 years of relevant work experience. Education may substitute for experience on a year for year basis. Experience with clinical data entry and medical terminology. Certified Clinical Research Coordinator (CCRC) or certification eligible Certified Clinical Research Professional (CCRP) or certification eligible Collaborative Institutional Training Initiative (CITI) training certification Oncology experience. Experience with database software. Computer skills. Communication. Interpersonal. Organization. Attention to detail. Multi-tasking.

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