Clinical Research Coordinator I
University of South Florida • Tampa, FL3d • $53,000 - $62,000
Research Coordinator Jobs
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Clinical Research Coordinator
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Clinical Research Coordinator I
University of South Florida•Tampa, FL
•$53,000 - $62,000
About The Position
The Clinical Research Coordinator I provides support to a lead coordinator or coordinates simple-to-moderately complex projects at the site level. The role conducts clinical trial visits and patient assessments, supports participant screening, enrollment, and retention, and collects study data. Depending on assigned protocols, assessments may include phlebotomy, sample processing, vital signs, ECGs, and other delegated clinical procedures, with coordination involving vendors, other departments, or outside facilities. The coordinator helps implement study protocols, collaborates with study and clinical teams, prepares site documents, and supports monitoring visits, audits, and inspections. The role also helps maintain site inventory, follows up with vendors and retrieves study-related records and reports, and monitors study activity for compliance with protocols, site SOPs, and applicable regulations, including HIPAA. The position provides guidance to less experienced site staff and performs other duties as assigned.
Requirements
- Bachelor's degree in a related field or an equivalent combination of education and experience.
- Must meet all U.S. employment eligibility requirements.
Responsibilities
- Support the lead coordinator or coordinate and lead simple-to-moderately complex projects at the site level.
- Perform clinical assessments for trial visits and coordinate with vendors, other departments, or outside facilities as needed.
- Participate in screening, enrollment, and retention of study participants.
- Conduct study visits and collect data throughout the research study.
- Assist with implementing assigned study protocols and related site activities.
- Communicate and collaborate with the study team and clinical team delegated to site-specific protocols.
- Collaborate on preparing and submitting site study documents.
- Assist with coordinating, preparing for, and conducting site monitoring visits, audits, and inspections.
- Help maintain site inventory, order research or laboratory materials, and follow up with vendors on items such as lab reports and medical records.
- Monitor site clinical study activity for compliance with the protocol, site SOPs, and applicable regulations, including HIPAA.
- Provide guidance to less experienced staff at the site.
- Perform other duties as assigned.
Benefits
- Medical insurance
- Dental insurance
- Life insurance
- Retirement plan options
- Employee and dependent tuition programs
- Generous leave
- Employee perks and discounts
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
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