CORE Clinical Research Crd 2

Tampa General Hospital • Tampa, FL

137d

About The Position

A Clinical Research Coordinator 2 (CRC 2) is a research professional responsible for managing all 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.

Requirements

• Bachelor's degree in science, Business Administration or health-related field.
• 3 to 5 years of experience as a Clinical Research Coordinator/Associate managing clinical research studies.
• Training in Phlebotomy within 3 months of hire if no prior experience.
• Experience in neurosciences or neurosurgery preferred.

Responsibilities

• Manage day-to-day activities of clinical trials.
• Recruit, screen, and enroll participants.
• Obtain informed consent and conduct study visits.
• Perform protocol required procedures as permitted by policy.
• Evaluate feasibility of proposed new trials.
• Review protocols to assess time and effort required for research staff.
• Track all study visits and validate financial reports.
• Reconcile and close out completed clinical trials.
• Prepare study specific source documents.
• Monitor safety and rights of participants.
• Document required data in the sponsor’s data capture tool.
• Report adverse and serious adverse events to the Principal Investigator and study sponsor.
• Act as a liaison between the site, study sponsor, and Principal Investigator.

What This Job Offers

• Career Level: Mid Level
• Education Level: Bachelor's degree