Remote Clinical Data Coordinator

Care Access; Boston (MA); A distancia; USD 36.000 - 50.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

PTO and holidays

Medical, dental, and vision insurance

HSA and FSA

Descripción de la vacante

Care Access is seeking a detail-oriented Data Coordinator to join our remote US team. You will support data quality across clinical trials, perform EDC/CRF data entry, and manage queries to keep study data accurate and inspection-ready.

Responsibilities include site-level quality control, data reconciliation, and study coordination across multiple sites. The role requires 2+ years in clinical research data coordination, strong communication, and the ability to work independently in a remote

Formación

• Minimum high school diploma or GED required; associate or bachelor’s degree preferred.
• 2+ years in clinical research, clinical trial support, healthcare operations, data coordination, or related role.
• Experience with electronic data capture systems and data entry.
• Experience reviewing, reconciling, and maintaining structured data using electronic systems.

Responsabilidades

• Perform site-level data quality control and clarify discrepancies with clinical staff.
• Reconcile study data against supporting documentation and maintain source materials.
• Enter study data into Sponsor EDC/CRF systems accurately and on time.
• Manage EDC queries, route and resolve items to move data toward closure.
• Coordinate with study teams to maintain data workflows and timelines.
• Support additional data quality, reporting, and documentation tasks as needed.

Conocimientos

Attention to detail

Data quality

Communication

Independent work

Educación

High school diploma or GED

Associate degree

Bachelor’s degree in life sciences / healthcare / clinical research / data management

Herramientas

EDC/CRF systems

Spreadsheets

Data trackers

Descripción del empleo

Care Access is seeking a detail-oriented Data Coordinator to join our remote US team. You will support data quality across clinical trials, perform EDC/CRF data entry, and manage queries to keep study data accurate and inspection-ready.

Responsibilities include site-level quality control, data reconciliation, and study coordination across multiple sites. The role requires 2+ years in clinical research data coordination, strong communication, and the ability to work independently in a remote