Clinical Study Coordinator

Job Description (Clinical Study Coordinator)

• Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations.
• Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance.
• Abstract medical information from various sources in the patient medical record.
• Report adverse events to medical monitor, FDA, and all other governing bodies.
• Coordinate all external audits and monitoring visits and serve as liaison between institution and sponsor.
• Serve as departmental and system-wide resource.

EDUCATION/EXPERIENCE REQUIRED:

Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two (2) years of relevant experience preferred.

CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.