Temporary Clinical Research Coordinator

Description

This position is grant funded. This position requires a level II background check.

The University of South Florida is a top-ranked research university serving approximately 50000 students from across the globe at campuses in Tampa St. Petersburg and USF 2025 U.S. News & World Report recognized USF with its highest overall ranking in university history as a top 50 public university for the seventh consecutive year and as one of the top 15 best values among all public universities in the nation. U.S. News also ranks the USF Health Morsani College of Medicine in the highest tier placing it as one of the top 16 medical schools in the nation and inside the top 10 among public universities. USF is a member of the Association of American Universities (AAU) a group that includes only the top 3% of universities in the U.S. With an all-time high of $750 million in research funding in 2025 and as a top 20 public university for producing U.S. patents USF uses innovation to transform lives and shape a better future. The university generates an annual economic impact of nearly $10 billion for the state of Florida. USFs Division I athletics teams compete in the American Conference. Learn more at .

Plans organizes and manages the resources necessary to achieve clinical research projectgoals and objectives at a single site.
Coordinates and performs patient clinical assessments for clinical trial visits for assigned clinicaltrial protocols including scheduling with vendors which may include other departments or outsidefacilities. This may include phlebotomy sample processing vitals ECGs and other delegatedclinical assessments per assigned protocols.
Communicates as a site representative with study sponsors third party vendors clinical teamsand patients to ensure all protocol required elements are being completed and collected within thedefined windows.
Ensures site compliance with research protocols reviews case report forms and audits foraccuracy with source documents attends site monitoring meetings with sponsors.
Manages the site research project databases develops flowsheets and other study relateddocuments 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 inregard to clinical research processes at the site.

Minimum Qualifications:

Bachelors degree in a related field -OR- equivalent combination of education and experience.

Preferred Qualifications:

Minimum of two (2) years of related experience

Senate Bill 1310- The Florida Senate ( is conditional upon meeting all employment eligibility requirements in the U.S.

SB 1310: Substitution of Work Experience for Postsecondary Education Requirements
A public employer may include a postsecondary degree as a baseline requirement only as an alternative to the number of years of direct experience required not to exceed:
(a) Two years of direct experience for an associate degree;
(b) Four years of direct experience for a bachelors degree;
(c) Six years of direct experience for a masters degree;
(d) Seven years of direct experience for a professional degree; or
(e) Nine years of direct experience for a doctoral degree

Related work experience may not substitute for any required licensure certification or registration required for the position of employment as established by the public employer and indicated in the advertised description of the position of employment.

Minimum Qualifications that require a high school diploma are exempt from SB 1310.

Required Experience:

IC