Clinical Research Coordinator (CRC) - Per Diem Onsite - Salt Lake City Area

Clinical Research Coordinator (CRC) – Per Diem Onsite – Salt Lake City Area Updated: Yesterday Location: Morrisville, NC, United States Job ID: 25107733 Description Illingworth Research Group provides patient‑focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. Services include mobile research nursing, patient concierge, medical photography and clinical research services. With experience across all study phases and a range of therapeutic areas, Illingworth operates in over 45 countries, bringing research directly into patients’ homes to improve their trial experience. Job Responsibilities Review assigned protocols and related documentation for accuracy, feasibility, timing, and resources. Prepare and maintain Investigator Site File and/or Trial Master File (TMF). Participate in creation and review of timelines and start‑up meetings (Investigator Meeting/SIV, Sponsor discussions, or related meetings). Lead and coordinate all required start‑up activities, including clinic logistics planning, schedule of clinic activities, team training, and preparation of study documents (CRFs, lab workbooks, staff schedules, etc.). Assist the Principal Investigator with study tasks such as delegation of authority log, daily task management, visit calendar development, monitor visit scheduling, and participant recruitment. Clinical Conduct Perform all study activities following Good Clinical Practices (GCP). Manage multiple clinical trials simultaneously; protect the safety of human subjects. Collect and enter study data into the appropriate system, complete CRFs, facilitate audits, and develop patient rapport to minimize protocol violations. Coordinate and monitor screening activities and informed consent. Take overall coordination of clinic activities, providing on‑call support when required. Post‑Clinic/Close‑Out Activities Resolve QC, monitor, CRF, or other findings. Oversee close‑out of study documentation, deviation reporting, and final study/volunteer logs. Ensure completion of other close‑out activities such as study supply return, IRB reports, and archiving. Prepare for and participate in sponsor/monitor/QA audits. Provide timely project status updates to Project Managers and sponsors. Accommodate flexible schedule, including days, afternoons, nights, and weekends. Coordinate and Perform Regulatory Activities Maintain proper protocol, consent, amendment, and yearly renewal submissions. Report adverse events related to the trial. Maintain study files. Travel up to 100%

QUALIFICATION REQUIREMENTS

Registered Nurse and/or University Degree such as Bachelor of Science. Clinical Research certification preferred. Minimum 1 year of clinical research experience, preferably in project coordination (2+ years preferred). Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines. Problem solving, planning, and evaluation skills. Time management, detail‑oriented, and multitasking abilities. Good interpersonal and communication skills with a team focus. Knowledge of SOP writing. Ability to anticipate problems and provide timely solutions. Ability to coordinate multiple clinical research projects with competing deadlines. Proficiency with Word, Excel, PowerPoint; experience with clinical trial EDC software preferred. Disclaimer Tasks, duties, and responsibilities listed in this job description are not exhaustive. The Company may assign other tasks, duties, and responsibilities. Equivalent experience, skills, or education will be considered for qualification. The company is committed to compliance with the Americans with Disabilities Act, including reasonable accommodations. Benefits Benefits may include a company car or car allowance, Health (Medical, Dental, Vision), Company match 401(k), Employee Stock Purchase Plan eligibility, performance‑based commissions/bonus, flexible paid time off, and sick time (subject to state and municipal requirements). Salary Range $67,700.00 – $115,100.00 The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on qualifications, skills, competencies, and proficiency for the role. Summary Coordinates or co‑leads assigned clinical research projects in accordance with Protocols, SOPs, and applicable regulations. #J-18808-Ljbffr Syneos Health, Inc.