Clinical Research Coordinator

Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection. Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation. Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care. Support study activities to facilitate smooth operations and accurate data management. Role: Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection. Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation. Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care. Support study activities to facilitate smooth operations and accurate data management. Responsibilities Coordinate clinical trial activities, including patient recruitment, informed consent, visit scheduling, and data collection. Ensure compliance with GCP, IRB, and sponsor regulations through accurate regulatory documentation. Collaborate with investigators, clinicians, and patients to promote safety, data integrity, and patient-centered care. Support study activities to facilitate smooth operations and accurate data management. Qualifications & Skills Attention to detail and strong organizational skills. Knowledge of clinical research protocols, regulatory requirements, and ethical standards. Ability to work collaboratively in a team environment. Excellent communication skills to interact effectively with stakeholders. #J-18808-Ljbffr