CORE Clinical Research Coordinator 2

Tampa General Hospital; Tampa (FL); On-site; USD 60,000 - 90,000; Full time

Job summary

Tampa General Hospital is seeking a Clinical Research Coordinator 2 to manage day-to-day activities of multiple clinical trials at the Tampa Main Campus. You will handle recruitment, screening, enrollment, informed consent, and protocol-required procedures, while ensuring data quality and participant safety.

The CRC 2 serves as a liaison among study sponsors, investigators, and hospital departments, ensuring compliance with federal regulations and hospital policies.

Qualifications

• Bachelor's Degree in Science, Business Administration or Health-related field.
• 3–5 years of experience as a Clinical Research Coordinator/Associate independently managing a portfolio of studies.
• All team members to receive Phlebotomy training within 3 months of hire if not already trained.

Responsibilities

• Manage day-to-day activities of clinical trials including recruitment, screening and enrollment of participants.
• Obtain informed consent, conduct study visits and perform protocol-required procedures.
• Maintain source documents, monitor safety/rights of participants and report adverse events.

Education

Bachelor's Degree in Science/Business Administration/Health-related field

Job description

Job Description - CORE Clinical Research Coordinator 2 (260003DS)

CORE Clinical Research Coordinator 2 - ( 260003DS )

Description

A Clinical Research Coordinator 2 (CRC 2) is a research professional responsible for managing all the day-to day activities of clinical trials, including but not limited to, recruitment, screening, enrollment of participants, obtaining informed consent, conducting study visits and performing protocol required procedures as permitted by policy and delegated by the Principal Investigator. A CRC 2 can perform the majority of tasks independently and perform quality checks on their own work. A CRC 2 focuses on ways to ensure retention of clinical trial participants; evaluates the feasibility of proposed new trials; reviews protocols to assess time and effort required of assigned research staff to ensure an accurate budget is created; tracks all study visits, reviews and validates the generated financial reports; reconciles and closes out completed clinical trials according to established federal regulations and guidelines. The CRC 2 prepares study specific source documents; continuously monitors the safety and rights of the participants, documents all required data in the sponsor's data capture tool and reports all adverse and serious adverse events that occur during the course of the trial to the Principal Investigator and the study sponsor. The CRC 2 is a liaison between the site, the study sponsor, and the Principal Investigator, as well as between the ancillary departments within the Office of Clinical Research and with other departments/clinics within the hospital or hospital system. Responsible for performing job duties in accordance with mission, vision and values of Tampa General Hospital.

Qualifications

• Bachelor's Degree Science, Business Administration,Health-related field
• Thee (3) to five (5) years of experience as a Clinical Research Coordinator/Associate independently managing a portfolio of clinical research studies and their participants.
• ALL team members required to receive training in Phlebotomy within 3 months of hire, if no prior Phlebotomy experience.

Primary Location

Tampa

Work Locations

TGH Main Campus 1 Tampa General Circle Tampa 33601

Eligible for Remote Work

On Site

Job

Clinical Research

Organization

Scheduled Days : Monday, Tuesday, Wednesday, Thursday, Friday