Attend study setup meetings to determine QC criteria and timelines for each study
Review study-specific source documents to ensure all forms are accurate prior to study start and
Ensure QC reviews are complete in accordance with study-specific timelines
Review source data on an ongoing basis to ensure clinical source data is complete according to GCP
Ensure data corrections are completed according to GCP guidelines and Celerion SOPs/PGs
Complete a Final QC to ensure all source data is accounted for and has been QC reviewed

🎯 Requirements

High School Diploma or GED (relevant internal Celerion experience in lieu preferred)
1 - 2 years industry experience preferred
Previous Quality Control/ Data Entry or related experience preferred
Medical Terminology Training preferred
Excellent oral and written communication skills
Ability to organize and manage multiple priorities

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