Similar Jobs
See allDirector, Clinical Quality - Program and Process Quality
Praxis Precision Medicines
US
GCP
CAPA
Risk Management
Senior Director, Quality
Care Access
US
GCP
CSV
Quality Management
Healthcare Compliance Director
Equip
US
Healthcare Compliance
Clinical Operations
Risk Assessment
Director, Clinical Site Operations
Bristol Myers Squibb
US
GCP
CRO
Clinical Operations
Director of Clinical Quality and Training
Sprinter Health
US
Quality Management
Training
Clinical
Responsibilities:
- Develop, execute, and optimize cost effective, phase-appropriate, QA compliance programs.
- Support international clinical trials through quality oversight, program/study team consultation, and QbD risk assessment.
- Collaborate with cross-functional teams to address findings and implement corrective and preventive actions.
Qualifications:
- Bachelor’s degree in a scientific discipline is required.
- 12+ years of experience in GCP/GLP compliance and monitoring within the biotechnology or pharmaceutical industry.
- Demonstrated expertise in critical thinking, influence, negotiation, problem solving, strategic thinking and leadership.
Kyverna Therapeutics
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, we are committed to transforming the future of treatment for autoimmune disease.