[Remote] Sr. Clinical Scientist

Note: The job is a remote job and is open to candidates in USA. Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company advancing cell therapies for autoimmune diseases. They are seeking a Senior Clinical Scientist who will support the design, execution, and analysis of clinical studies in accordance with GCP and regulatory requirements, while collaborating cross-functionally to drive high-quality study execution.ResponsibilitiesSupport the design, development, and execution of clinical studies, with accountability for protocols, clinical documents, and overall study quality in alignment with GCP and regulatory expectations. Including but not limited to:Performing comprehensive, ongoing review of clinical trial data (e.g., safety, efficacy, adverse events, laboratory data)Identifying data trends, discrepancies, and potential safety signals; escalating findings appropriatelyGenerating, tracking, and resolving data queries in collaboration with data management and clinical operationsEnsuring accuracy, completeness, and consistency of clinical data across systems and reportsParticipating in study start-up and oversight activities, including vendor management and CRO collaborationContribute to site-facing activities, including investigator support, training, and query resolutionProactively identify risks and implement mitigation strategies, particularly in areas such as enrollment, site performance, and operational executionParticipate in the development, writing, and review of key clinical and regulatory documents, including protocols, clinical study reports, informed consent forms, safety updates, and submission materialsSupport clinical data review and interpretation, including safety and efficacy dataMaintain deep understanding of program data and evolving clinical insightsSupport publication and data dissemination strategies, including development of abstracts, presentations, and manuscriptsSkillsAdvanced scientific degree required (PhD, PharmD, MD, or equivalent)2+ years of experience in clinical research within biotech or pharmaceutical environments, with a strong preference for candidates who have operated in early-stage or build-phase companiesDemonstrated ability to work independently and collaboratively in ambiguous, fast-moving environments with limited infrastructureStrong understanding of GCP, clinical trial design, and regulatory requirements, with the ability to balance scientific rigor, compliance, and practical executionExperience with electronic data capture (EDC) systems (e.g., Medidata RAVE or similar); prior involvement in data query management and data cleaning activities preferredExperience with clinical data review, including safety, efficacy, and/or laboratory data, and familiarity with statistical approachesHands-on experience with data visualization software (e.g., GraphPad Prism)Excellent written and verbal communication skills, with the ability to distill complex scientific information and influence cross-functional stakeholdersHigh attention to detail and strong organizational skillsWillingness to travel as needed to support clinical sites, investigator meetings, and scientific conferencesExperience in autoimmune disease, immunology, neurology, or hematologyBenefitsBonusBenefitsEquity participationCompany OverviewKyverna Therapeutics is pioneering a new class of therapies and cures for serious autoimmune diseases. It was founded in 2018, and is headquartered in Berkeley, California, USA, with a workforce of 51-200 employees. Its website is http://kyvernatx.com.Company H1B SponsorshipKyverna Therapeutics has a track record of offering H1B sponsorships, with 1 in 2025, 1 in 2023, 1 in 2021. Please note that this does not guarantee sponsorship for this specific role.