Clinical Research Coordinator I — Site Operations

University of South Florida in; Tampa (FL); On-site; USD 52,000 - 64,000; Full time

Job summary

The Clinical Research Coordinator I at University of South Florida coordinates and performs research activities for clinical trials, overseeing screening, enrollment, retention, and data collection under the direction of lead coordinators and principal investigators.

This is a time-limited position not eligible for visa sponsorship and requires a related bachelor’s degree or an equivalent combination of education and experience, with responsibilities including adherence to study protocols and

Qualifications

• Bachelor's degree in a related field or equivalent combination of education and experience.

Responsibilities

• Provides direct support to lead coordinator or coordinate and serve as project lead for projects that are simple to moderate in complexity at the site level.
• 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. Participates in the screening, enrollment, and retention of study participants at the site.
• Conducts study visits and data collection throughout research study.
• Assist with implementation of procedures and activities of assigned study protocols at the site.
• Communicates and collaborates with the study team and clinical team delegated on site specific protocols.
• Collaborates with the preparation and submission of site study documents.
• Assist with coordination, preparation, and conduct of site monitoring visits, audits and inspection.
• Assist with site inventory maintenance (order materials necessary for research projects or lab activities) and other vendor follow-up items (lab report retrieval, medical record retrieval).
• Monitor clinical study activity at the site to ensure compliance with the protocol, site SOPs (Standard Operating Procedures) and all applicable regulations, including HIPAA (Health Insurance Portability and Accountability Act) regulations.
• Provides guidance to less experienced staff at the site.
• Performs other duties as assigned.

Education

Bachelor's degree in related field or equivalent combination of education and experience

Job description

The Clinical Research Coordinator I at University of South Florida coordinates and performs research activities for clinical trials, overseeing screening, enrollment, retention, and data collection under the direction of lead coordinators and principal investigators.

This is a time-limited position not eligible for visa sponsorship and requires a related bachelor’s degree or an equivalent combination of education and experience, with responsibilities including adherence to study protocols and