Associate Director, Clinical Quality Assurance
Listed on 2026-10-09
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Quality Assurance - QA/QC
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Healthcare
Medical Science, Data Scientist
Role:
Associate Director of Clinical Quality Assurance overseeing GCP compliance for Centessa-sponsored early to late-phase clinical trials in neurology, focusing on narcolepsy and sleep disorders.
Responsibilities: lead GCP QA programs, conduct and manage audits of investigational sites, CROs, and systems, develop audit strategies, support regulatory inspections, and ensure documentation and process adherence. Collaborate with cross-functional teams on protocol design, risk management, and training; monitor evolving GCP regulations, and lead quality improvement initiatives.
Qualifications:
BS or higher in Life Sciences, Chemistry, Pharmacy, with 8-10 years in pharmaceutical quality roles. Experience with document control software (e.g., Veeva Vault, ZenQMS) required.
High-Value: clinical QA for GCP compliance, regulatory inspection readiness, early to late-phase trials, neurotherapeutics, in US-based role with occasional travel.
Work setup: full-time, US-based, remote with travel.
Are you ready to take on the Associate Director, Clinical Quality Assurance role at Scorpion Therapeutics?
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