Central Study Coordinator I

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.

Through 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, Care Access puts people at the heart of medical progress.

How This Role Makes a Difference

Central Clinical Services enables decentralized and hybrid clinical trials by providing virtual staff support to patients and research sites. The Central Study Coordinator (CSC) combines clinical research and project management expertise into a single role that delivers strong customer experience for both patients and sites.

As a virtual extension of the research site, the CSC supports one to four sites concurrently across one or more studies. You will be accountable for study delivery at the patient level, including screening, consenting, and conducting protocol-mandated study visits. The role requires patient-centric practices and a quality-first approach.

Key Responsibilities

• Support patient screening, enrollment, and informed consent processes
• Conduct protocol-mandated study visits and follow-up activities
• Serve as primary liaison between Care Access, research sites, and patients
• Manage daily work using patient-centric practices and quality-first standards
• Act as project manager for assigned studies in collaboration with Principal Investigators
• Support site coordination across multiple concurrent studies
• Maintain study documentation and regulatory compliance

About You

You bring a combination of clinical research experience, strong organizational skills, and genuine commitment to patient care. Ideal candidates demonstrate excellent communication abilities, ability to manage multiple priorities, and experience in clinical trial coordination or related healthcare settings.