Specialist II, Quality Compliance

Role: Quality Specialist II, supporting clinical GCP compliance and audit readiness within Corcept's clinical operations. Responsibilities: assist with vendor qualification, monitoring, and audits; support inspection readiness initiatives; maintain audit documentation and metrics; participate in GCP audits; develop process improvements; and track quality performance metrics. Requirements: BA/BS in biological sciences, pharmacy, or related field; 2-4 years’ experience in clinical-stage pharma or related industry; proficiency in Microsoft Office; basic GCP knowledge. HighValue: clinical GCP compliance, audit coordination, vendor oversight, inspection readiness, quality metrics, biopharma (clinical-stage), headquartered in California with up to 25% travel; hybrid work setup at least 3 days/week.