Priovant Therapeutics

The role ensures the delivery of investigational products to global clinical studies through packaging, labeling, and distribution management. It involves coordinating with external partners and monitoring enrollment trends to maintain an uninterrupted product supply.

The role focuses on ensuring compliant documentation of clinical study activities and developing Quality Systems for clinical development programs. Key duties include serving as the primary QA contact for Phase 3 studies, performing site audits, and managing study oversight metrics.

The Clinical Research Associate will conduct site visits and manage site activities to ensure compliance with regulatory guidelines and project timelines. They will also interact with clinical site staff to resolve issues and ensure the validity of study data.