Supplier Performance Monitor

Job Summary

Monitoring supplier performance, the full-time Supplier Performance Monitor will evaluate compliance and data quality for clinical trials while developing relationships with external third-party suppliers in a remote capacity.

Key responsibilities:

• Monitoring the collection, processing, and analysis of data from external suppliers for clinical trials
• Evaluating supplier compliance and data quality, tracking corrective actions related to monitoring issues
• Developing professional relationships with external suppliers and stakeholders

Required qualifications:

• Doctorate, Master's, Bachelor's, Associate's degree, RN, or GED with relevant years of experience
• Laboratory auditing experience, preferably in in-vitro diagnostics
• 7 years of work experience in life sciences or a medically related field, including clinical research experience
• Technical knowledge of imaging, adjudication, or specialty laboratory testing
• Knowledge of Good Clinical Practice (GCP) and QA processes