Data Coordinator

The posting, as Care Access wrote it

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

Data Coordinators play an important role in clinical research by helping ensure study data is accurate, complete, and available when needed. As part of a centralized data coordination team, this role helps protect data integrity, and support Care Access’ mission to make clinical trials more accessible to participants everywhere.

Through source data quality control, accurate EDC/CRF transcription, visit-to-entry reconciliation, and proactive query follow-up, Data Coordinators help keep study records reliable and inspection-ready. By catching discrepancies early and helping move issues to resolution, this role contributes to smooth study operations across the Care Access site network.

How You'll Make An Impact

• Site-Level Quality Control:
• Review source data collected during clinic visits and work with clinical staff to clarify or resolve discrepancies before information is entered into Sponsor EDC/CRF systems. Responsibilities include:
• Reviewing source records for completeness, internal consistency, and required good documentation practices.
• Identifying missing data, incomplete fields, missing signatures, or other potential documentation issues.
• Reviewing source records for consistency with protocol requirements and study workflows.
• Documenting quality control activities in the approved Care Access system and tracking items through to resolution.
• Data Reconciliation:
• Reconcile study data against supporting documentation to make sure required source records are available, complete, and aligned with study expectations. Responsibilities include:
• Confirming availability of required source materials, including lab reports, ECGs, imaging reports, and other visit-related records.
• Reconciling visit documentation against required study data points and expected source records.
• Maintaining and reconciling adverse event information, informed consent logs, protocol de

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ection with an application for employment.
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Diversity & Inclusion

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com