Performs review of protocols, informed consents, and case reports forms (CRFs) prior to study
Performs audits of internal departments as required
Works directly with international coordinators and project managers to ensure accurate
Performs review of marketing and recruiting documentation
Performs audit of study material receipt and return/destruction
Performs in clinic monitoring of study procedures per associate clinical study

🎯 Requirements

Associates and min of 2 –4 years of relevant experience
Bachelor’s and min 1-3 years of relevant experience
Demonstrated ability to understand clinical studies
Excellent organizational, attention to detail, interpersonal skills, and possesses a high level of
Knowledge of GCP ICH/GLP guidelines and Federal Regulations related to the conduct of Clinical
Preferred: ISO 19011 Internal Auditing Training- preferred

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