Clinical Research Coordinator

CenExel•Salt Lake City, UT

10d•Onsite

About The Position

The Clinical Research Coordinator is responsible for coordinating all aspects of clinical trials while adhering to ICH, GCP, study protocols, and company guidelines, regulations, and policies. Under supervision, the coordinator supports patient involvement in complex and/or multiple studies from initiation through completion, organizes research information, schedules data collection, observes subjects, and assists with data analysis and reporting. The role also supports study administration, regulatory compliance, protocol development, participant education, and safety and efficacy assessments. The coordinator assists the Clinical Trial Manager with vendor oversight, accounting, regulatory activities, client satisfaction, recruitment, quality, trial outcomes, and staff planning, processes, training, and development. The schedule is Monday through Friday for 36 hours, with occasional weekends required. Shifts run from 6 a.m. to 6 p.m., with days varying according to study needs. Compensation is $22–$24 per hour, depending on experience, education, and skillset. The role is based in an indoor office environment and may require overnight travel for training or investigative meetings.

Requirements

Experience demonstrating mastery of the Clinical Research Coordinator I position.
Knowledge and understanding of federal regulations protecting human subjects in research and governing clinical trials.
Strong leadership and mentorship skills.
Ability to develop and maintain effective working relationships throughout the organization and with sponsors and vendors.
Crisis-management and problem-solving skills, including the ability to respond calmly and effectively in emergent situations.
Ability to work independently and as part of a team.
Effective verbal and written communication skills.
Ability to meet essential physical requirements, including sitting, typing, standing, walking, and occasional lifting of up to 20 pounds.
Ability to report to work as scheduled.
Ability to travel overnight for training and/or investigative meetings if required.

Nice To Haves

CCRC certification preferred.
Two to three years of experience in the medical field preferred.

Responsibilities

Coordinate patient involvement in complex and/or multiple studies from study initiation through completion.
Organize clinical-trial research information and schedule data collection.
Observe subjects and assist with data analysis and reporting.
Review and appropriately report adverse events, protocol deviations, and other unanticipated problems.
Monitor and report research data to maintain quality and compliance.
Perform administrative and regulatory duties related to studies as appropriate.
Participate in protocol development activities.
Ensure the site receives accurate information and supplies from sponsors, including source materials, protocols, scales, supplies, approvals, and contacts.
Educate potential participants and caregivers about protocol-specific details and expectations.
Perform protocol-required safety and efficacy assessments, including vital signs, EKGs, blood draws, and other assigned assessments.
Assist the Clinical Trial Manager with oversight of vendors, accounting, regulatory activities, client satisfaction, recruitment, quality, and trial outcomes.
Assist the Clinical Trial Manager with planning, process creation, training, and staff development.
Perform other assigned duties and responsibilities.