Clinical Research Coordinator — Manage Trials

University of Utah; Campus (IL); On-site; USD 42,000 - 65,000; Full time

Job summary

A prominent educational institution is seeking Clinical Research Coordinators (Non-R.N.) to oversee daily clinical trial activities, ensuring compliance with regulations and patient safety. Responsibilities include coordinating research procedures, obtaining informed consent, and maintaining documentation. Successful candidates typically hold a bachelor's degree with relevant experience in clinical research coordination. This role emphasizes patient interaction and adherence to Good Clinical Practices. Full benefits are provided, supporting a collaborative medical environment.

Qualifications

• Minimum of 4 years of experience in clinical research coordination.
• Experience in protocol review and understanding of regulatory compliance.
• Ability to work with diverse populations, focusing on patient safety.

Responsibilities

• Coordinate day-to-day clinical trial activities.
• Collect and maintain patient and laboratory data.
• Document and track adverse events accurately.

Skills

Clinical research coordination

Good Clinical Practices (GCP)

Informed consent procedures

Adverse event reporting

Regulatory documentation

Education

Bachelor's degree or equivalency + 4 years related work experience

Master's degree or equivalency + 2 years related work experience

Job description

A prominent educational institution is seeking Clinical Research Coordinators (Non-R.N.) to oversee daily clinical trial activities, ensuring compliance with regulations and patient safety. Responsibilities include coordinating research procedures, obtaining informed consent, and maintaining documentation. Successful candidates typically hold a bachelor's degree with relevant experience in clinical research coordination. This role emphasizes patient interaction and adherence to Good Clinical Practices. Full benefits are provided, supporting a collaborative medical environment.