Responsibilities:
- Support clinical study design and execution with accountability for protocols, documents, and quality in alignment with GCP and regulatory expectations.
- Perform ongoing data review to identify trends and safety signals, escalating findings appropriately and managing data queries.
- Participate in study start-up and oversight activities, including vendor management and CRO collaboration to drive high-quality execution.
Qualifications:
- Advanced scientific degree (PhD, PharmD, MD) required with 2+ years of experience in biotech or pharmaceutical clinical research.
- Demonstrated ability to work independently and collaboratively in ambiguous, fast-moving environments with strong GCP and regulatory understanding.
- Experience with EDC systems, data review, and visualization software, plus excellent communication and organizational skills.
Compensation:
- National salary range is $140,000 to $160,000 annually, with actual compensation based on experience, skills, and internal equity.
- Role is eligible for bonus, benefits, and equity participation, supporting a proactive and team-oriented work environment.
Kyverna Therapeutics
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company advancing cell therapies for autoimmune diseases. The company is building the foundation for the next generation of cell therapy with a culture guided by core values like staying true to purpose and bold innovation, operating at a critical scaling stage.