Clinical Research Coordinator

CenExel•Murray, UT

10d•$22 - $24•Onsite

About The Position

The Clinical Research Coordinator coordinates clinical trials from study initiation through completion, adhering to ICH, GCP, study protocols, company guidelines, regulations, and policies. The position works under supervision and coordinates patient involvement in complex and/or multiple studies, organizes clinical research information, observes subjects, supports data analysis and reporting, and schedules data collection. It also performs safety and efficacy assessments and administrative and regulatory duties, and supports the Clinical Trial Manager with operational oversight and staff development. The schedule is Monday through Friday, 36 hours per week, with occasional weekends required. The shift is 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 work is in an indoor office environment. Overnight travel may be required for training and/or investigative meetings.

Requirements

Must have proper experience and demonstrate mastery of the Clinical Research Coordinator I position.
Knowledge and understanding of federal regulations protecting human subjects in research and governing the conduct of clinical trials.
Strong leadership and mentorship skills.
Ability to develop and maintain effective working relationships at all levels of the organization and with sponsors and vendors.
Crisis management and problem-solving skills, including the ability to react calmly and effectively in emergent situations.
Ability to work independently and as part of a team.
Effective verbal and written communication skills.

Nice To Haves

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

Responsibilities

Under supervision, coordinate aspects of patient involvement for complex and/or multiple studies from study initiation through study completion.
Organize research information for clinical trials.
Observe subjects and assist with data analysis and reporting.
Schedule the collection of data.
Review and report adverse events, protocol deviations, and other unanticipated problems appropriately.
Monitor and report research data to maintain quality and compliance.
Perform administrative and regulatory duties related to studies as appropriate.
Participate in other 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 on protocol-specific details and expectations.
Perform safety and efficacy assessments per protocol, including vital signs, EKGs, blood draws, and other assigned assessments.
Assist the Clinical Trial Manager with oversight of vendors, accounting, regulatory matters, client satisfaction, recruitment, quality, and trial outcomes.
Assist the Clinical Trial Manager with planning, creating processes, training, and staff development.
Assume other duties and responsibilities as assigned.