
Clinical Research Coordinator
Manages screening, implements recruitment procedures, consenting, enrollment, randomization and study conduct from planning through study closeout. Performs or implements processes to assure study-related procedures are performed as required and objectives and timelines are met. Maintains accurate and timely documentation and communication with Investigators, participants, IRB, sponsors and other research related entities. With assistance, prepares and processes new IRB research proposals, amendments, continuing review applications and adverse event reports according to institutional and departmental policies and procedures and federal regulations. Prepares and maintains documents required to be maintained and available internally and for regulatory authorities and/or the sponsor prior to, during and after the conduct of a clinical/translational trial. Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures.
Ability to work in a fast paced environment
Strong understanding of the regulatory environment
1 year of related experience
MS Word
Time Management Skills
MS Excel skills
Data analysis and reporting skills
Process Improvement
Verbal communication
written communication
Problem Solving Skills
Multi tasker
Flexibility and adaptability
According to JobzMall, the average salary range for a Clinical Research Coordinator in 1211 Medical Center Dr, Nashville, TN 37232, USA is $45,000 to $62,000.
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The Vanderbilt University Medical Center is a medical provider with multiple hospitals in Nashville, Tennessee, as well as clinics and facilities throughout Middle Tennessee. VUMC is an independent non-profit organization, but maintains academic affiliations with Vanderbilt University.

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