CORE Clinical Research Coordinator 1

Tampa General Hospital; Tampa (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

Tampa General Hospital is seeking a Core Clinical Research Coordinator 1 to oversee day-to-day trial activities at the Tampa Main Campus. You will recruit and screen participants, obtain informed consent, and conduct study visits and protocol procedures under supervision.

Responsibilities include ensuring participant safety, collecting data in sponsor's data capture tools, and coordinating with sponsor, PI, and hospital departments while following federal regulations.

Qualifications

• 1–2 years of experience as a Clinical Research Coordinator/Associate or equivalent patient-facing clinical role.
• ALL team members required to receive Phlebotomy training within 3 months of hire if no prior Phlebotomy experience.
• Bachelor’s degree in science, business, or health-related field is required.

Responsibilities

• Manage day-to-day activities of clinical trials under supervision.
• Recruit, screen, and enroll participants; obtain informed consent.
• Conduct study visits and perform protocol-required procedures as permitted by policy.

Education

Bachelor's Degree Science

Bachelor's Degree Business Administration

Bachelor's Degree Health-related field

Job description

Job Description - CORE Clinical Research Coordinator 1 (260003WG)

Job Description

CORE Clinical Research Coordinator 1 - ( 260003WG )

Description

A Clinical Research Coordinator 1 (CRC 1) is a research professional who works under the guidance and supervision of their leader and is 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 1 focuses on ways to ensure retention of clinical trial participants; tracks all study visits, reviews and validates the accuracy of financial reports; works with Research Finance and Regulatory to reconcile all items necessary to close out completed clinical trials according to established federal regulations and guidelines. The CRC 1 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 1 works closely with the sponsor representatives and the Principal Investigator, as well as 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

Education Qualifications

• Bachelor’s Degree Science
• Bachelor’s Degree Business Administration
• Bachelor’s Degree Health-related field

Experience Qualifications

• One (1) to two (2) years of experience as a Clinical Research Coordinator/Associate managing a portfolio of clinical research studies and their participants OR one (1) year of relevant patient facing clinical experience (such as Nurse Aid, Patient Care Technician (PCT), Medical Assistant (MA), Phlebotomist).
• 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

Schedule

Full-time

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