About the job
About Care Access
At Care Access, we are committed to transforming the future of healthcare for everyone. With a global network of research sites, mobile clinics, and expert clinicians, we deliver top-tier research and health services to communities that frequently encounter obstacles to care. Our mission is to empower individuals to understand their health, access necessary care, and play a vital role in the medical advancements of tomorrow.
Through initiatives like Future of Medicine, which provides cutting-edge health screenings and research opportunities to communities worldwide, and Difference Makers, which aids local leaders in enhancing their community health efforts, we prioritize people in our quest for medical progress. By leveraging partnerships, innovative technology, and unwavering determination, we are redefining how clinical research and health services are delivered globally. Join us in our journey to create a healthier, more accessible future for all.
To learn more about Care Access, visit www.CareAccess.com.
Role Overview
The Clinical Research Coordinator I plays a crucial role by applying Good Clinical Practices (GCP) in screening, enrolling, and meticulously monitoring clinical research participants while ensuring adherence to protocols and regulatory standards.
Key Responsibilities
- Comprehend and adhere to institutional Standard Operating Procedures (SOPs).
- Evaluate and clarify protocol documents (including amendments) for logistical feasibility.
- Ensure completion of all training and study prerequisites before trial initiation.
- Collaborate with Investigators and site personnel to discuss study medications, required procedures, eligibility criteria, and their impact on office workflow.
- Assist in the development of effective recruitment materials.
- Support the creation of a recruitment strategy and compile a list of potential candidates from the subject database.
- Engage actively with the recruitment team to contact and recruit subjects.
- Participate in Investigator meetings as necessary.
- Coordinate and attend pre-study site visits, site initiation visits, and monitoring visits alongside clinical staff and Sponsors/CRO representatives.

