Clinical Research Coordinator (Req# 14299)
|April 25, 2012 - June 11, 2012|
|Employment Type:||Full Time|
|Department:||University Physician Associates Admin 1101|
|Description:||The primary responsibility of the Clinical Research Coordinator (CRC) is to manage all aspects of conducting clinical trials. The Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. |
|Duties:||Along with the investigator, the Clinical Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the Clinical Research Coordinator is responsible for all data and source documentation, adverse event reporting, and maintenance of complete regulatory files.|
|Qualifications:||MINIMUM REQUIRED EDUCATION – Bachelor’s degree, or graduate from an RN school of nursing, or equivalent medically-related education at an Associate’s degree level (LVN). Successful completion of Association of Clinical Research Professionals (ACRP) Certified Clinical Research Coordinator (CCRC) certification required within two years of eligibility.|
MINIMUM REQUIRED EXPERIENCE – One year of clinical research experience, or successful completion of UTHSCT Clinical Research Coordinator Internship.
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