CRC Associate
Core
Support clinical research activities to ensure high-quality data, protocol adherence, and patient safety by coordinating study conduct and managing documentation.
Role type
Clinical Research Coordinator (CRC) Associate
Builds
Clinical studies and trial data
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical coordination, patient screening, informed consent documentation, eCRF completion, TMF management, study visit scheduling, data query resolution
Preferred skills
Experience in clinical research or regulated environments, understanding of GCP guidelines
Technologies
Electronic Case Report Forms (eCRFs), Trial Master File (TMF)
Responsibilities
Support setup and day-to-day conduct of clinical studies; Assist with patient screening and enrolment; Ensure accurate completion of source documents and eCRFs; Organize and maintain study files and TMF content; Coordinate study visits and patient appointments; Collaborate with monitors and investigators to resolve data queries
Seniority
Entry-level to Junior, hands-on IC