CCRC (Certified Clinical Research Coordinator), CCRP (Certified Clinical Research Professional)
Academic / Research
Position Summary: The Clinical Research Coordinator conducts research activities following all federal regulations and Good Clinical Practice guidelines. Responsible for orchestrating all activities involving the recruitment and enrollment of study patients and managing the critical study documentation and data collection necessary for each protocol.
We are a warm and welcoming practice. All of our coordinators have been here for over 5 years.
Position Responsibilities and Expectations:
Screen and enroll study subjects ensuring compliance with enrollment criteria and facilitate completion of the informed consent document.
Perform and/or schedule various study implementation methods and procedures based on protocol and coordinates various clinical activities between departments and other clinical specialists.
Maintain source documentation for all data submitted, including clinic or PI/Sub-I visit chart notes, lab reports, and procedure reports.
Perform technical and professional clinical procedures.
Perform follow-up activities of eligible subjects according to protocol requirements (e.g. subject follow-up, case report form completion, and reporting of adverse drug experiences and protocol deviations).
We look forward to speaking more at your interview.
LIVING IN PALM BEACH COUNTY NEED ONLY APPLY
Email all resumes to JACKERMAN@CCTLLC.NET and Lwyatt@cctllc.net
Comprehensive Clinical Trials has been conducting research studies since 2000. Comprehensive Clinical Trials is one of the most technologically advanced and accomplished clinical research sites in the United States. Comprehensive Clinical Trials is a preferred research facility for the largest pharmaceutical companies globally.