Clinical Research Coordinator-256633

Position OverviewThe Clinical Research Coordinator will ensure execution of assigned clinical trials in compliance with GCP, ICH, HIPAA, FDA regulations, and company SOPs. Operates independently while practicing ALCOA principles, maintaining strict confidentiality, and upholding high integrity.Key ResponsibilitiesScreen and consent subjects; conduct visit scheduling, appointment reminders, and follow-ups; collect vital signs/ECGs; perform lab procedures (phlebotomy, centrifuging, specimen storage/shipping/accountability, and courier notification).Document in source clinic charts; build/update source files; perform EDC data entry and query resolution; update logs and chart filings; maintain and order study supplies; request/track medical records.Complete start-up tasks (training, ISF filing); prepare for and attend SIVs and Investigator Meetings (IMs); set up and maintain study technology; host monitoring visits and resolve issues; ensure investigator review of lab/patient results; file SAEs/Deviations to Sponsor and IRB; report adverse events and non-compliance promptly.Assist with recruitment and tracking; maintain positive communication with team members and clients; perform other duties as assigned.Qualifications & SkillsMA diploma, LPN/LVN, EMT credential, or Associate’s degree and 1+ years of clinical research or clinical experience (or an equivalent combination).Preferred proficiency in basic clinical skills (blood pressure, vitals, EKGs, phlebotomy).Computer proficiency (MS Office, email, EHR, web applications)