Clinical Research Coordinator

Intermountain Health Intermountain Medical Center

Full time

R177521

This on-site position serves as a Subject Matter Expert (SME) in clinical research and is responsible for the coordination and management of clinical studies at Intermountain Healthcare. Working in a patient-facing environment, this role collaborates closely with clinical investigators, physicians, department leadership, regulatory coordinators, sponsors, and other stakeholders to ensure the efficient execution of research studies, regulatory compliance, and high-quality participant care throughout the research process.

• Core business hours: Monday–Friday, 8:00 a.m. – 5:00 p.m.

• 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 Standard Operating Procedures (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.

• Research Protocols

• Independent worker and self-starter

• Critical thinking and decision making

• Detail-oriented

• Personable

• Highly organized

• Documentation /p

• Verbal and written communication

• Patient information

• Clinical Information systems

• Experience in a role requiring the ability to demonstrate proficiency 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.

• Three (3) years of experience in a clinical research role requiring use of laboratory protocol, systems and documentation techniques, detailed knowledge of human subject research regulations, strong demonstrated attention to detail and ability to adhere to policies and procedures.

• Demonstrated experience working in a collaborative team environment.

• Experience using word processing, spreadsheet, database, internet and e-mail and scheduling applications.

• Experience in a role requiring effective organizational skills; effective follow-through, and commitment to excellence, effective professional communication skills;
  Ability to communicate with others in a clear, understandable, and professional manner as well as strong interpersonal skills:
  Ability to work with personnel at all levels to gather information, communicate compliance requirements and handle complex issues within an often-sensitive political environment.

• Extensive professional experience in a clinical research role requiring use of laboratory protocol, systems and documentation techniques, detailed knowledge of human subject research regulations, strong demonstrated attention to detail and ability to adhere to policies and…