Clinical research coordinator manages clinical trial performance and ensures conduct is congruent to company policy. Promote good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federal regulations and company guidelines for the enrollment and maintenance of subjects in clinical trials, and by collecting, recording and maintaining source and sponsor documentation.
understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start up meeting, and coordinating with the principal investigator.
Adhere strictly to the study protocol; Obtain exemptions when necessary/appropriate
Communicate protocol issues to CRO/Sponsor, Site Administrator, Director, Principal or Sub-Investigators.
Collect initial Psychiatric and medical information by interviewing patients and by accessing other appropriate sources.
Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, and specimen packaging.
Maintain timely company source documentation as well as Sponsor required information.
Dispense and maintain accurate records of study medication.
Complete all Sponsor and monitor queries in a timely manner.
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