Support clinical research studies by coordinating participant recruitment, screening, scheduling, and study visits. Assist physicians and research nurses in delivering high-quality patient care while ensuring compliance with study protocols, FDA regulations, and Good Clinical Practice (GCP) standards. Manage study documentation, data collection, laboratory processes, and communication with sponsors, investigators, and regulatory agencies. Play a key role in maintaining participant safety and contributing to the successful completion of clinical trials.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED