Clinical Research Coordinator- 258517

We are seeking a Clinical Research Coordinator to manage clinical study protocols across their full lifecycle, from start-up through closeout. In this part-time role, you will work independently or in close collaboration with research nurses to oversee participant scheduling, conduct patient-facing visits, drive EDC data management, and support site regulatory requirements. You will play a vital operational role ensuring all study activities comply strictly with FDA regulations, ICH guidelines, and Good Clinical Practice (GCP).

Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below.
Schedule: Part-Time, 20 hours per week (Monday – Friday between 8:00 AM – 5:00 PM; no evenings or weekends)
ResponsibilitiesCoordinate assigned clinical research protocols from study startup through closeout, serving as the sole coordinator or partnering with a research nurse.Identify, screen, and enroll eligible trial participants, coordinating the full schedule of protocol events from screening through follow-up.Conduct patient-facing study activities and visits in accordance with protocol guidelines.Manage end-to-end clinical trial data in Electronic Data Capture (EDC) systems, including data abstraction, query resolution, tracking, SAE and lab data reconciliation, and safety coding.Prepare and manage essential regulatory documents, IRB submissions, and protocol compliance tracking.Serve as the primary operational site liaison for sponsors and CROs, including triggering trial-related financial payments.Participate in site feasibility evaluations, Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), and team research meetings, while supporting recruitment of new trials to the site.
Required SkillsProven experience as a Clinical Research Coordinator (CRC) handling protocols from startup to closeout.Strong working knowledge of FDA regulations, ICH guidelines, Good Clinical Practice (GCP), and IRB regulatory requirements.Hands-on proficiency with Electronic Data Capture (EDC) systems, data entry, query resolution, and safety/SAE reconciliation.Experience with participant screening, recruitment, schedule-of-events management, and direct patient-facing trial visits. xzbcwsv Ability to work an on-site, 20-hour-per-week schedule during standard business hours.