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Responsibilities:
- Support site activities and timelines.
- Ensure clinical trial compliance.
- Participate in data cleaning activities.
Oversight Activities:
- Provide oversight of CRO CRAs.
- Maintain study Trial Master File.
- Perform regular TMF review and QC checks.
Additional Support:
- Contribute to study documents and training materials.
- Partner with patient operations.
- Support inspection readiness.
Kyverna Therapeutics
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. They are committed to transforming the future of treatment for autoimmune disease by staying true to their values and innovating boldly.