Clinical Research Coordinator – Vascular Trials

University of Utah; Salt Lake City (UT); Presencial; USD 39.000 - 73.000; Jornada completa

Descripción de la vacante

The University of Utah Health is seeking a Clinical Research Coordinator for the Vascular Surgery Development division on the Campus in Salt Lake City, UT. This full-time role focuses on coordinating clinical research studies under IDE/IND requirements and maintaining study integrity.

You will oversee recruitment, consent, data collection, and regulatory documentation while collaborating with investigators and sponsors. Strong organization and knowledge of GCP/IRB are essential.

Formación

• Bachelor's degree in health sciences or related field; equivalency allowed.
• Two years professional research experience required.
• Completion of University RATS Clinical Certification within one year of hire.

Responsabilidades

• Screen and recruit participants for clinical research studies.
• Obtain and document informed consent; draft consent documents under supervision.
• Attend study team meetings and assume leadership roles.
• Schedule visits and coordinate facility/equipment availability.
• Assess protocols for clarity and participant safety; review criteria.
• Collect and document clinical data and maintain study documentation.
• Report and track adverse events to PI, IRB and sponsor.
• Review and manage clinical study databases.
• Educate staff on study procedures.
• Document protocol deviations and reconcile test article accountability.

Conocimientos

Organizational skills

Attention to detail

Communication skills

GCP knowledge

IRB regulations knowledge

Educación

Bachelor's degree in health sciences or related field

Two years professional research experience

University RATS Clinical Certification within 1 year

Descripción del empleo

The University of Utah Health is seeking a Clinical Research Coordinator for the Vascular Surgery Development division on the Campus in Salt Lake City, UT. This full-time role focuses on coordinating clinical research studies under IDE/IND requirements and maintaining study integrity.

You will oversee recruitment, consent, data collection, and regulatory documentation while collaborating with investigators and sponsors. Strong organization and knowledge of GCP/IRB are essential.