Senior Clinical Research Coordinator — Onsite Study Expert

Intermountain Health; Columbia (SC); On-site; USD 34,000 - 55,000; Full time

Job summary

Intermountain Medical Center in Murray, Utah, is seeking a Senior Clinical Research Coordinator to oversee coordinating and managing clinical studies in a patient-facing environment, ensuring regulatory compliance and high-quality participant care.

This role emphasizes mentorship of Coordinators I, adherence to GCP and SOPs, data management, and collaboration with investigators, sponsors, and staff to drive study success.

Qualifications

• Experience with Microsoft and database applications.
• Experience using laboratory protocol, systems and documentation techniques.
• Demonstrated experience in a healthcare, academics or research related setting or research related setting working with patients.

Responsibilities

• Research Support: Support various research studies across the Intermountain system, working on complex or large projects with limited supervision, demonstrating high competency in clinical research.
• Mentorship: Provide support and mentorship to Clinical Research Coordinators I, reinforcing training and knowledge of study protocols and procedures.
• Education: Educate and disseminate information about research projects, communicating with study teams and physicians about protocols and timelines.
• Compliance: Utilize GCP guidelines for screening, assessing participant eligibility, conducting study procedures, data entry, and patient monitoring, and participate in oversight visits.
• Recruitment: Helps facilitate strategies for study recruitment, participant retention, and study execution, performing ongoing quality assurance and evaluations at study completion as requested.
• Information Management: Ensure compliance with best practices for transmitting patient information as required by study approvals and protocols, supporting study team and investigator adherence to GCP guidelines.
• Training: Complies with and trains clinical research coordinator 1 on basic techniques of clinical research coordination, FDA Good Clinical Practices (GCP), and clinical research SOPs, maintaining compliance with Intermountain policy, research sponsors, and Federal regulations.
• Laboratory Operations: Collect, process, maintain, and ship lab samples, demonstrating laboratory competency and compliance with SOPs.
• Performs other duties as assigned (e.g., data entry, expense tracking, patient chart reviews).
• May be required to take on-call assignments, work weekends and overtime.

Skills

Research Protocols

Independent worker

Critical thinking

Detail-oriented

Personable

Highly organized

Documentation

Verbal and written communication

Patient information

Clinical Information systems

Education

Bachelor's Degree in clinical or life science

Job description

Intermountain Medical Center in Murray, Utah, is seeking a Senior Clinical Research Coordinator to oversee coordinating and managing clinical studies in a patient-facing environment, ensuring regulatory compliance and high-quality participant care.

This role emphasizes mentorship of Coordinators I, adherence to GCP and SOPs, data management, and collaboration with investigators, sponsors, and staff to drive study success.