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Job description
Akebia Therapeutics is seeking an Associate Director, Research and Development Quality Assurance to lead GCP/GLP/GVP compliance across trials. The role requires collaboration with clinical development, medical affairs, and safety teams to ensure regulatory readiness and risk mitigation.
Responsibilities include audits, CAPAs, and oversight of contracted auditors, with a focus on sustainable quality across programs. Hybrid in-office options are available based on role and business needs.
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Worksite address
waltham, MA, 02254, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.