Temporary Clinical Research Coordinator

University of South Florida•Tampa, FL

About The Position

This position is grant funded and requires a level II background check. The University of South Florida (USF) is a top-ranked research university serving approximately 50,000 students. USF is recognized for its high rankings by U.S. News & World Report, its membership in the Association of American Universities (AAU), and its significant research funding and economic impact. USF's Morsani College of Medicine is also highly ranked nationally. The university is a major employer in the Tampa Bay area, dedicated to cultivating a talented and driven workforce.

Requirements

Bachelor's degree in a related field -OR- equivalent combination of education and experience.
Senate Bill 1310- The Florida Senate is conditional upon meeting all employment eligibility requirements in the U.S.
Applicants for USF employment are entitled to request reasonable accommodation(s) in the application process.

Nice To Haves

Minimum of two (2) years of related experience

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.