Clinical Research Coordinator - Full-Time

Role Overview: The Clinical Research Coordinator (CRC) supports clinical studies under a principal investigator, performing hands-on procedures, community outreach, and ensuring compliance with protocols and Good Clinical Practice (GCP) guidelines. Key Responsibilities Perform clinical procedures such as ECG, sample collection, and vital signs.Coordinate study activities, prepare materials, set up equipment, and manage logistics.Recruit, screen, and orient patients, ensuring their safety and well-being.Accurately collect and record clinical data in case report forms (CRFs).Collaborate with investigators and monitors to address queries and maintain data quality.Act as a patient advocate and uphold safety standards according to policies. Qualifications & Skills Bachelor’s degree preferred or relevant experience.At least 1+ years of experience in clinical research.Knowledge of clinical trials, GCP, and medical terminology.Detail-oriented with strong relationship-building skills.Proficiency with EDC systems, data entry, and query management. Additional Notes: This on-site role is not eligible for sponsorship. Compensation ranges from $35.00 to $42.00 per hour, with potential additional benefits. IQVIA values diversity and is an equal opportunity employer.