Clinical Research Coordinator II

About Care Access Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all. To learn more about Care Access, visit www.CareAccess.com. How This Role Makes a Difference The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance. How You'll Make An Impact Coordination and Conduct of Clinical Trials Study Planning and Scheduling: Prioritizing tasks according to study protocol timelines. Managing scheduling conflicts between visits and procedures through close collaboration with Investigators, nurses, and the PSC. Regulatory Compliance: Adhering to FDA and ICH GCP guidelines in clinical trial conduct. Ensuring all study procedures are performed in accordance with Good Clinical Practice (GCP) standards. Maintaining knowledge of and compliance with internal Care Access SOPs in daily activities. Collaboration with the Study Team and Participants: Professional communication with the Principal Investigator (PI), study staff, and Sponsor/CRO representatives. Close cooperation with investigators and the study team, supporting investigators and nurses during patient visits, and ensuring patient documen tation is prepared prior to visits.