Clinical Research Coordinator II — On‑Site Trials

Intermountain Healthcare Inc.; Salt Lake City (UT); On-site; USD 39,000 - 61,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

Intermountain Health in Salt Lake City, UT is seeking a Clinical Research Coordinator to support and coordinate complex studies across the Intermountain system, partnering with physicians, investigators, and sponsors to ensure regulatory compliance and high-quality participant care.

The role emphasizes training, data entry, patient monitoring, and recruitment strategies under GCP guidelines, with on-site hours and occasional travel.

Qualifications

• Three years of clinical research experience with lab protocols and documentation.
• Knowledge of human subject regulations and compliance requirements.
• Attention to detail and ability to adhere to procedures.

Responsibilities

• Support various research studies across the Intermountain system with limited supervision.
• Provide mentorship and training to junior coordinators on study protocols.
• Educate teams about timelines, procedures, and regulatory requirements.
• Utilize GCP guidelines for screening, enrollment, data entry, and monitoring.
• Facilitate recruitment strategies and ensure study execution and QA.

Skills

Research protocols

Independent worker

Detail oriented

Communication skills

Team collaboration

Clinical information systems

Education

Bachelor's degree preferred

Tools

GCP guidelines

Job description

Intermountain Health in Salt Lake City, UT is seeking a Clinical Research Coordinator to support and coordinate complex studies across the Intermountain system, partnering with physicians, investigators, and sponsors to ensure regulatory compliance and high-quality participant care.

The role emphasizes training, data entry, patient monitoring, and recruitment strategies under GCP guidelines, with on-site hours and occasional travel.