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Responsibilities:
- You will serve as the primary Clinical QA point of contact for a Phase 3, global study.
- You will collaborate with cross-functional groups to support study start-up and execution.
- You will perform clinical site audits and support inspection readiness.
Qualifications:
- You have a Bachelor's degree in life sciences with 6-12 years of biopharmaceutical experience.
- You have experience in GCP Quality and the ability to audit independently.
- You possess strong communication, problem-solving, and decision-making skills.
About Priovant:
- Priovant is a biopharmaceutical company committed to developing therapies for autoimmune diseases.
- The team operates with a hands-on, collaborative approach and a high sense of urgency.
Priovant
Priovant is a biopharmaceutical company committed to developing therapies for autoimmune diseases. They have a small, collaborative team with a hands-on culture.