Clinical Research Coordinator 258764

Medix™; Little Rock (AR); On-site; USD 52,000 - 70,000; Full time

Job summary

Medix in Little Rock, AR is seeking a Clinical Research Coordinator to manage participant enrollment and study visits, ensuring informed consent and compliance with protocol requirements.

You will collect patient data, record vital signs, process specimens, and handle data entry into case report forms, while monitoring safety and reporting adverse events. You’ll serve as the primary contact for sponsors and laboratories, ensuring regulatory standards are met.

Qualifications

• Must follow Good Clinical Practice (GCP) guidelines, FDA regulations, and Institutional Review Board (IRB) rules.
• Collects patient data, records vital signs, processes lab specimens, and enters information into case report forms or databases.

Responsibilities

• Recruit, screen, and enroll eligible patients and obtain informed consent.
• Collect patient data, record vital signs, process lab specimens, and enter data into case report forms or databases.
• Ensure study compliance with GCP, FDA regulations, and IRB rules.
• Track, document, and report adverse events or side effects.
• Serve as the main contact for sponsors and liaise with laboratories.

Job description

• Participant Management: Recruits, screens, and enrolls eligible patients; obtains informed consent; and coordinates study visits.
• Data and Record Keeping: Collects patient data, records vital signs, processes lab specimens, and enters information into case report forms or databases.
• Regulatory Compliance: Ensures the study follows Good Clinical Practice (GCP) guidelines, FDA regulations, and Institutional Review Board (IRB) rules.
• Safety Monitoring: Tracks and reports adverse events or side effects experienced by participants.
• Communication: Acts as the primary point of contact for patients, answers sponsor queries, and liaises with laboratories