Clinical Research Coordinator; CRC - Per Diem - Salt Lake Area

Syneos Health, Inc.

Ogden, UTPosted May 8, 2026

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Qualifications

  • •Registered Nurse and/or university degree such as Bachelor of Science required
  • •Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines
  • •Problem‑solving, planning, and evaluation skills
  • •Excellent time management, detail‑oriented, and multitasking ability
  • •Good interpersonal and communication skills with a team focus
  • •Knowledge of SOP writing
  • •Ability to anticipate problems and provide solutions promptly
  • •Ability to coordinate multiple projects with competing deadlines
  • •5 more items(s)

Responsibilities

  • •Clinical Research Coordinator (CRC) – Per Diem – Salt Lake City Area
  • •Review assigned protocols and other protocol documentation for accuracy, feasibility, timing, and resources
  • •Prepare and maintain the Investigator Site File and/or Trial Master File (TMF) for the study
  • •Participate in creation and review of timelines and start‑up meetings (Investigator Meeting/SIV, sponsor discussions, or other related meetings)
  • •Take lead and/or overall coordination of all required start‑up activities, including clinic logistics planning, schedule of clinic activities, team training, preparation and review of clinic source documents, time and event tables, case report forms, lab workbooks, staff requirements, schedules, safety assessment requirements, QC and monitoring plans, pharmacy/dispensing requirements, study supplies, meal plans, and regulatory/contractual documentation
  • •Support the Principal Investigator with tasks such as delegation of authority log, daily task management, visit calendar development and maintenance, scheduling and attending monitor visits, advertising, recruiting, and screening potential participants
  • •Perform all study activities following Good Clinical Practice (GCP) and manage multiple clinical trials simultaneously
  • •Protect the safety of human subjects and monitor for updates in clinical study or federal regulations
  • •Collect and enter study data into the appropriate system and submit data within required time frames
  • •Coordinate and monitor screening activities; assist with informed consent; facilitate audits and develop patient and team rapport to minimize protocol violations
  • •Take lead/overall coordination of clinic activities, including supervising clinic visits, screening eligibility, overseeing study drug administration, ensuring all study-related activities follow protocol, SOP, and regulations, and managing clinic updates, adverse events, logs, trackers, QC, and monitor findings
  • •Coordinate resolution of QC, monitor, CRF, or other returns; oversee close‑out of documentation, deviation reporting, and study logs; update TMF; finalize volunteer logs; ensure completion of return of supplies, IRB reports, archiving, etc
  • •Prepare for and participate in sponsor/monitor/QA audits and provide accurate project status updates to project managers and sponsor
  • •Collaborate during process improvement, SOP creation, internal/external meetings, and company initiatives; accommodate flexible schedule
  • •Perform other work‑related duties as assigned
  • •Maintain protocol, consent, amendment, and yearly renewal submissions
  • •Report adverse events related to the trial
  • •Maintain study files
  • •15 more items(s)
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