Data Compliance Coordinator
Core
Support the management and delivery of UK clinical studies at the Manchester research site, acting as a link between sponsors and the site.
Role type
Data Compliance Coordinator (Clinical Research)
Builds
Clinical trial data integrity and regulatory compliance for UK studies
Domain
Life Sciences / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
ICH/GCP guidelines knowledge, eCRF data entry, query resolution, Investigator Site Files (ISF) maintenance, data protection regulations, Microsoft Office, medical terminology
Preferred skills
Experience with monitoring visit preparation, quality control capabilities, time management for multiple studies
Technologies
eCRF, Microsoft Office
Responsibilities
Manage and maintain accurate clinical study and patient data, Complete electronic Case Report Form (eCRF) data entry and resolve data queries, Maintain Investigator Site Files (ISF) and other essential study documentation, Coordinate data management and compliance activities across multiple studies, Prepare for monitoring visits and support timely follow-up actions, Perform quality checks to maintain high standards of data accuracy, completeness and integrity
Seniority
Entry-level to Junior, hands-on IC
