Priovant Therapeutics · 11 hours ago
Senior Associate/Manager, Quality
Priovant is committed to developing therapies that address high unmet need in autoimmune disease. The Associate / Manager, Quality will help advance this mission by ensuring complete and compliant documentation of clinical study activities and developing Quality Systems across Priovant's clinical development programs.
Biotechnology
Responsibilities
Track, upload, and manage documentation required to be in the TMF across studies. This includes working with internal and external collaborators to obtain documentation, respond to queries, and track TMF health
Collaborate with other quality and clinical operations staff on study oversight metric input and review. Additionally, create action plans for metrics that exceed KPIs
Use metrics to identify clinical study sites with higher than desired clinical risk and work to mitigate these risks
Perform clinical site, TMF, and/or vendor site audits, as needed
Support clinical site inspection readiness
Develop and implement procedures for the Priovant Therapeutics Quality Management System (QMS)
Qualification
Required
Bachelor's degree in one of the life sciences, or equivalent knowledge and experience
6-12 years of experience in biopharmaceutical industry or related field with experience in GCP Quality, experience in additional GXP disciplines a plus
Organized and thorough, with attention to details
Hands-on, roll-up-your-sleeves approach, with a high sense of urgency and drive for results
Demonstrated communication, problem-solving, and decision-making skills
Natural collaborator who enjoys working on a cross-functional team
Company
Priovant Therapeutics
Priovant Therapeutics is a clinical-stage biotechnology company focused on delivering novel therapies.
Funding
Current Stage
Growth StageRecent News
Spherix Global Insights
2025-10-10
Seattle TechFlash
2025-09-25
BioWorld Financial Watch
2025-09-20
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