Senior Compliance Coordinator
Core
Ensures accurate capture of study documentation and source data in eCRFs, performs quality reviews, and manages Investigator Site Files (ISF) for clinical trials.
Role type
Senior Compliance Coordinator (Clinical Trials)
Builds
Study documentation, eCRF data integrity, and audit readiness for clinical trials
Domain
Healthcare / Clinical Research / Regulatory Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial documentation knowledge, eCRF management, ISF verification, GCP/ICH/GCP regulations, audit preparation, data entry accuracy, protocol deviation reporting, CAPA identification
Preferred skills
Medical terminology, multi-tasking, commercial and patient confidentiality, MS Office
Technologies
eCRF systems, ISF trackers, MS Office
Responsibilities
Maintain ISF and study trackers, verify ICF completion, assist with data capturing across multiple sites, track eCRF flow and queries, report protocol deviations, assist monitors with query resolutions, support audit preparation, identify data errors and trends
Seniority
Senior, hands-on IC
