Clinical Research Coordinator — Impactful, Full-Time Trials

Rocky Mountain Clinical Research; Idaho Falls (ID); On-site; USD 23,000 - 34,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401(k) retirement plan

Paid time off (PTO)

Job summary

Rocky Mountain Clinical Research in Idaho Falls, ID is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team. The CRC will work with the Principal Investigator and study staff to conduct trials in compliance with GCP and FDA regulations.

This position offers an hourly wage of $17–$25, a benefits package including medical/dental/vision, a 401(k), PTO, and opportunities for professional growth in a patient-focused clinical research setting.

Qualifications

• Healthcare or medical background (clinical or patient-facing experience).
• Strong clerical, organizational, and documentation skills.
• Excellent interpersonal and communication skills.
• High attention to detail and commitment to quality and accuracy.
• Ability to work independently while collaborating effectively with a team.

Responsibilities

• Coordinate and administer clinical trials under the direction of the Principal Investigator
• Screen, enroll, consent, and follow study participants
• Ensure participant safety and protocol adherence throughout the study lifecycle
• Maintain accurate source documentation and regulatory files
• Complete study-related data entry and follow-up documentation with high attention to detail
• Prepare for and support sponsor, monitor, and regulatory audits
• Collaborate with investigators, sponsors, monitors, and internal research staff
• Ensure studies are conducted in compliance with GCP, FDA regulations, and study protocols

Skills

Healthcare background

Clerical & docs

Interpersonal skills

Attention to detail

Independent yet team-oriented

Education

CMA / LPN / RN or higher credentialing

Job description

Rocky Mountain Clinical Research in Idaho Falls, ID is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team. The CRC will work with the Principal Investigator and study staff to conduct trials in compliance with GCP and FDA regulations.

This position offers an hourly wage of $17–$25, a benefits package including medical/dental/vision, a 401(k), PTO, and opportunities for professional growth in a patient-focused clinical research setting.