Clinical Research Study Coordinator

University of Utah; Salt Lake City (UT); On-site; USD 60,000 - 90,000; Full time

Job summary

University of Utah is seeking a Clinical Research Coordinator to oversee coordination of clinical or research studies, ensuring protocol adherence and data integrity under the supervision of the Principal Investigator.

The role involves coordinating study logistics, informed consent, subject safety, and collaboration with sponsors, IRB, and study teams to meet objectives and timelines.

Qualifications

• Bachelor's degree in a related field or equivalency.
• IRB CITI Course in the Protection of Human Research subjects within six months.
• Vaccination requirements must be fulfilled or approved for exemption.

Responsibilities

• Assesses protocol for clarity and subject safety, reviews criteria; clarifies concerns with PI and sponsor.
• Attends and participates in Investigator and staff meetings; advises team on assignments and timelines.
• Explains and obtains informed consent, medical history and demographics; documents in source files.
• Determines visit lengths and coordinates related facility and equipment availability.
• Reports adverse events to IRB and sponsor; tracks deviations and prepares summaries for sponsor.
• Completes, audits, corrects CRFs and relays CRFs to sponsor.
• Assists with negotiating contract budget and payment terms.
• Maintains documents per FDA guidelines; may submit IRB documents.
• May coordinate specimen collection, processing and shipment.
• Performs duties as a Clinical Research Assistant when needed.

Skills

Communication skills

Education

Bachelor's degree in a related field

IRB CITI Certification

IATA DGR training

Job description

University of Utah is seeking a Clinical Research Coordinator to oversee coordination of clinical or research studies, ensuring protocol adherence and data integrity under the supervision of the Principal Investigator.

The role involves coordinating study logistics, informed consent, subject safety, and collaboration with sponsors, IRB, and study teams to meet objectives and timelines.