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Responsibilities:
- Support the design, specifications, and development of eCRFs
- Develop Data Management Plan documents
- Perform comprehensive review of data generated from the clinical study
Qualifications:
- Bachelor’s degree in life sciences, health informatics, or related field
- 8+ years of Clinical Data Management experience in a CRO / Pharma setting
- Proficient in data cleaning and query resolution techniques
Compliance:
- Ensure CDM activities are performed in compliance with Good Clinical Practice, ICH Guidelines, Kyverna SOPs, regulatory guidelines, and study specific plans.
- Support the filing of eTMF documentation to ensure that an inspection ready environment is maintained
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 and redefining what’s possible.