Responsible for developing data management plans and validating/testing databases
Review and track clinical trial data for completeness, accuracy, and consistency
Manage and prioritize data management activities to meet project schedules
Train and mentor Clinical Data Associate(s)
Lead database cleaning and lock activities, coordinating with QA or data quality reviews.
Requirements
Bachelor’s degree in a scientific discipline
At least 5 years of clinical data management experience in the pharmaceutical/biotechnology industry
Highly detail-oriented while maintaining work efficiency
Ability to prioritize activities and multi-task across various projects
MedDRA and WHO Drug coding proficiency preferred
Previous experience with reviewing data and database validation for EDC required (Viedoc EDC preferred)
Knowledge of CDISC/SDTM standards highly desired
Must reside and work in the PST, MST, or CST time zone or be local to San Diego County.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data management plansdatabase validationclinical trial data reviewdata cleaningdata quality reviewsMedDRA codingWHO Drug codingEDCCDISC standardsSDTM standards