Manage clinical study data remotely from Canada, combining database oversight with study coordination and quality control responsibilities. Work alongside international colleagues and sponsor teams.
Warman O’Brien is recruiting a Clinical Data Manager for an established international Contract Research Organisation. You will own data management activities across assigned studies, supporting timely delivery and compliance. The work includes CRFs, eCRFs, edit checks, query management, and database lock readiness.
Key Responsibilities:
Coordinate clinical data activities across the study lifecycle
Develop and review CRFs, eCRFs, specifications, and edit checks
Review data, identify discrepancies, and oversee query resolution
Maintain data flow, quality control, and study documentation
Support database QC, closure, pre-lock checks, and lock readiness
Requirements:
Three to five years of relevant clinical data management experience
BSc in Life Sciences, Health Sciences, or related scientific discipline
Experience owning clinical study data management activities
Practical experience with electronic data capture systems
Knowledge of standards, regulations, and SOP-driven processes
Bring clinical data management, EDC, query, and database lock expertise to internationally delivered studies from Canada.
J-18808-Ljbffr