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University of South Florida · 10 hours ago

Clinical Research Coordinator II - Temporary

Florida, United States

Part-time

Onsite

Entry, Mid Level

2+ years exp

The University of South Florida is a top-ranked research university dedicated to cultivating a talented workforce. They are seeking a Clinical Research Coordinator II to manage clinical research projects, ensuring compliance with protocols and quality data collection throughout studies.

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Responsibilities

Plans, organizes, and manages the resources necessary to achieve clinical research project goals and objectives at a single site

Coordinates and performs patient clinical assessments for clinical trial visits for assigned clinical trial protocols including scheduling with vendors which may include other departments or outside facilities. This may include phlebotomy, sample processing, vitals, ECGs and other delegated clinical assessments per assigned protocols

Communicates as a site representative with study sponsors, third party vendors, clinical teams and patients to ensure all protocol required elements are being completed and collected within the defined windows

Ensures site compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends site monitoring meetings with sponsors

Manages the site research project databases, develops flowsheets and other study related documents, and completes source documents/case report forms

May provide guidance to other clinical research staff and support personnel

Makes recommendations of procedures in order to facilitate protocol compliance

Performs data entry and query resolution during the duration of each trial assigned

Serve as a resource for both internal and external customers and members of the community in regard to clinical research processes at the site