Supplier Performance Management Monitor
On-site · Raleigh, North Carolina, United States or Blue Bell, Pennsylvania, United States
Job Summary
Monitor and evaluate data collection and analysis from external third-party suppliers for sponsored clinical trials; assess supplier compliance and data quality; track corrective actions related to monitoring issues and audits; build professional relationships with external suppliers and stakeholders; requires advanced degrees and substantial related experience in life sciences/clinical research; emphasizes data integrity, GCP knowledge, QA processes, CAPA, auditing, and metrics to drive quality in biopharmaceutical clinical trials.
Required Qualifications
- Doctorate/Masters/BA/BS/RN/AD/GED
- Laboratory auditing experience
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