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Senior Director, Clinical Science
Kyverna Therapeutics. Serve as the senior clinical scientist for CAR T-cell therapy clinical trials in autoimmune disease indications, in partnership with internal and external cross-functional teams .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading clinical trials for CAR T-cell therapy, with a strong focus on regulatory compliance, strategic execution, and cross-functional collaboration. Possesses advanced knowledge in drug development, particularly in late-stage clinical trials and cell and gene therapy.
Highest-signal resume keywords
CAR T-Cell TherapyClinical Trial DesignRegulatory SubmissionsDrug DevelopmentImmunology
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ExecutionClinical Development PlansStudy ProtocolsInvestigator BrochuresRegulatory ComplianceGCP ComplianceClinical Study ReportsSafety UpdatesData InterpretationProgram-Level Strategy
Soft Skills
Exceptional CommunicationManagement SkillsOperational AcumenMentoringCollaboration
Certifications & Qualifications
Ph.D.Pharm.D.M.D.
Industry Keywords
Autoimmune DiseaseCell and Gene TherapyGlobal Regulatory FrameworksClinical Development PathwaysLate-Stage Clinical Trials
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Serve as the senior clinical scientist for CAR T-cell therapy clinical trials in autoimmune disease indications, in partnership with internal and external cross-functional teams
- Partner with clinical operations, biometrics, regulatory, and commercial teams to ensure alignment on strategy and execution
- Lead design, execution, and interpretation of clinical trials across the assigned program
- Provide scientific input into clinical development plans, study protocols, investigator brochures, and regulatory submissions
- Participate in developing clinical trial documents, including protocols, ICFs, clinical development plans, and publications
- Lead development of clinical sections of regulatory documents, including the IB, safety updates, clinical study reports, and responses to Health Authorities in collaboration with the study physician
- Represent Clinical Development for the assigned program with cross-functional leaders, key opinion leaders, strategic partners, and external stakeholders
- Represent Clinical Development in advisory boards, regulatory meetings, and major congresses, as appropriate
- Contribute to external scientific narrative and positioning through publications, presentations, and collaborations
- Ensure compliance with GCP, corporate policies, and applicable local regulations
- Lead, mentor, and develop clinical scientists and other staff
- Foster a culture of innovation, accountability, and scientific rigor
- Contribute to Clinical Development organizational design and capability building to support future pipeline growth and complexity
Requirements
What you’ll need- Advanced degree (Ph.D., Pharm.D., M.D., or equivalent) in a scientific or life sciences discipline required
- 10+ years of progressive experience in drug development, including significant experience across multiple programs, including late-stage global clinical trials
- Demonstrated success in developing and executing clinical strategies at a program level
- Experience in late-stage clinical trials required
- Experience in cell and gene therapy, immunology, autoimmune disease, or related fields strongly preferred
- Deep understanding of global regulatory frameworks and clinical development pathways required
- Strong operational acumen with excellence and efficiency
- Exceptional communication and management skills
- Ability to operate independently and effectively in a fast-paced, highly dynamic environment
- Ability to travel up to 15% of the time
Benefits
Comp & perks- Annual bonus eligibility
- Equity
- Benefits
- Participation in the Company’s stock plan