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The Operational Compliance Specialist ensures operational quality compliance in clinical trials, driving process improvement, overseeing CAPA actions, and providing training on GCP and compliance topics.

Develop and maintain software applications for Care Access, focusing on full-stack development using TypeScript and collaborating with cross-functional teams. Lead technical discussions and ensure high-quality deliverables while supporting production systems.

The Specialist in Study Training Compliance manages training completion and DOA matrices for clinical research studies, ensuring compliance and regulatory adherence. This involves tracking staff training, maintaining records, and supporting audits while collaborating with stakeholders to ensure seamless operations.