Elevate your career as a Clinical Data Coordinator specializing in Phase I–III trials. This role entails ensuring data quality and compliance within multi-regional clinical studies, particularly in the UK and LATAM.

As a Senior Clinical Data Coordinator, you'll play a vital role in managing and verifying clinical trial data throughout its lifecycle. Your collaboration with various teams, including programming and safety departments, is essential in maintaining high data standards. This position demands a proactive approach to troubleshoot discrepancies and support timely data resolution to meet study milestones.

Key Responsibilities:
• Conduct comprehensive reviews to identify data discrepancies
• Oversee the reconciliation of critical data streams




• Develop and follow up on data queries to enhance quality
• Perform User Acceptance Testing for database integrity
• Ensure compliance with GCP and regulatory standards

Requirements:
• At least 3 years in clinical data coordination
• Bachelor's degree in Life Sciences or related fields
• Robust experience with EDC systems
• Preferred experience in clinical data review processes
• Understanding of CDISC standards advantageous

Utilize your clinical coordination expertise to contribute to the success of global clinical trials.
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📌 Clinical Data Coordinator for Phase I–III Trials (Alberta)
🏢 Inductive Quotient Analytics
📍 Alberta