Nurse

The Clinical Study Coordinator supports the execution of clinical trials by ensuring all study activities are conducted in compliance with FDA, ICH-GCP guidelines, and study protocols. The role focuses on patient safety, accurate data collection, and smooth site operations.Key Responsibilities:Conduct clinical trial procedures including informed consent, screening, vital signs, ECGs, and sample collectionSchedule and manage participant visits within protocol timelinesEnsure accurate and timely data entry in case report forms (CRFs) and electronic systems (EDC)Maintain source documents, patient records, and regulatory filesMonitor patient safety and report protocol deviations or non-complianceSupport participant recruitment, enrollment, retention, and follow-upsCoordinate with site staff, investigators, and sponsorsEnsure IRB approvals and regulatory compliance throughout the studyHandle patient communication, appointment confirmations, and educationRequirements:Bachelor’s degree in a clinical/medical fieldValid nursing license (RN/LVN/LPN)Minimum 2+ years of relevant clinical or research experienceSkills:Strong knowledge of clinical research (GCP, SOPs, safety monitoring)Attention to detail, organization, and problem-solving abilitiesGood communication and teamwork skillsBasic computer proficiency