A company is looking for a Clin Trials Monitor / Auditor.
Key Responsibilities
Perform comprehensive audits and monitoring of clinical trials, ensuring protocol compliance and reviewing regulatory documents
Verify timely reporting of Serious Adverse Events (SAE) and protocol deviations to applicable regulatory agencies and internal organizations
Generate audit and monitoring reports summarizing findings of deviations, discrepancies, and missing data, and provide training as needed
Required Qualifications
Bachelor's degree in biology, chemistry, biochemistry, physiology, nursing, or related fields
Two or more years of experience as a Clinical Research Associate or clinical trial auditor / monitor
Clinical Trials Auditor • Manchester, New Hampshire, United States