Clinical Research Coordinator

Rocky Mountain Clinical Research; Idaho Falls (ID); Sur place; USD 23 000 - 34 000; Plein temps

Avantages offerts par ce poste

Medical, dental, and vision insurance

401(k) retirement plan

Paid time off (PTO)

Résumé du poste

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.

Responsabilités

• 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

Connaissances

Healthcare background

Clerical & docs

Interpersonal skills

Attention to detail

Independent yet team-oriented

Formation

CMA / LPN / RN or higher credentialing

Description du poste

Clinical Research Coordinator (Full-Time)

Rocky Mountain Clinical Research Idaho Falls, ID

Rocky Mountain Clinical Research is seeking a full-time Clinical Research Coordinator (CRC) to join our growing team in Idaho Falls, ID. This is an excellent opportunity for a healthcare professional looking to expand into clinical research while making a meaningful impact on patient care and the future of medicine.

Compensation & Benefits

• Hourly wage: $17 – $25 per hour (based on education, training, and experience)
• Benefits package includes:
  • Medical, dental, and vision insurance
  • 401(k) retirement plan
  • Paid time off (PTO)
• Full-time, stable position with opportunities for professional growth

About Rocky Mountain Clinical Research

Rocky Mountain Clinical Research was founded on the principle of advancing medical care for patients facing complex diseases. We conduct high-quality clinical research across a range of therapeutic areas, including diabetes, evaluating medications and medical devices to determine their safety and effectiveness compared to current standards of care.

As an investigator-led, patient-focused research site, we play a key role in bringing new treatments to market while ensuring patient safety and regulatory compliance. We are a family-oriented organization that values teamwork, integrity, and long-term employee success.

Position Summary: Clinical Research Coordinator

The Clinical Research Coordinator plays a critical role in the day-to-day execution of clinical trials. Working closely with the Principal Investigator, Research Director, and study team, the CRC ensures that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), and federal regulations.

This role combines patient interaction, clinical coordination, and administrative responsibilities, making it ideal for detail-oriented healthcare professionals who enjoy both people-facing and organizational work.

Key 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

Required 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

Preferred Qualifications

• Certified Medical Assistant (CMA), Licensed Practical Nurse (LPN), Registered Nurse (RN), or higher credentialing
• Experience in a healthcare, research, or clinical trial environment
• Familiarity with Good Clinical Practice (GCP), clinical trial protocols, or regulatory documentation
• Strong analytical and decision-making skills

Clinical research experience is preferred but not required- GCP and CRC training will be provided for motivated candidates.

Work Schedule

• Full-time
• Monday – Friday
• Occasional (but rare) weekends or major holidays required

Location: 83404