Care Access
Teams at Care Access
Recently posted jobs
Other
Lead operations and performance for multiple clinical research sites across a region, ensuring GCP/FDA/ICH compliance, timely enrollment, data quality, budget oversight, staff leadership and development, stakeholder management, audits, and risk mitigation. May perform Clinical Research Coordinator duties at sites as needed.
Other
The Central Study Coordinator - Retention manages patient interactions, educates on lab results, coordinates study participation, and ensures participant retention for clinical trials.
Other
The Source Document Specialist ensures accurate clinical trial documentation by translating protocols into structured source documents, validating accuracy, managing version control, and supporting global research operations.
