Senior Clinical Research Scientist

Kyverna Therapeutics

Senior Clinical Research Scientist at Kyverna advancing cell therapies for autoimmune diseases. Driving high-quality study execution and optimizing clinical processes in a fast-paced environment.

Posted 5/1/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $140,000 - $160,000 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support 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 appropriately
Generating, tracking, and resolving data queries in collaboration with data management and clinical operations
Ensuring accuracy, completeness, and consistency of clinical data across systems and reports
Participating in study start-up and oversight activities, including vendor management and CRO collaboration
Contribute to site-facing activities, including investigator support, training, and query resolution
Proactively identify risks and implement mitigation strategies, particularly in areas such as enrollment, site performance, and operational execution.
Participate in the development, writing, and review of key clinical and regulatory documents, including protocols, clinical study reports, informed consent forms, safety updates, and submission materials.
Support clinical data review and interpretation, including safety and efficacy data
Maintain deep understanding of program data and evolving clinical insights
Support publication and data dissemination strategies, including development of abstracts, presentations, and manuscripts.

Requirements

What you’ll need

Advanced 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 companies.
Demonstrated ability to work independently and collaboratively in ambiguous, fast-moving environments with limited infrastructure
Strong understanding of GCP, clinical trial design, and regulatory requirements, with the ability to balance scientific rigor, compliance, and practical execution.
Experience with electronic data capture (EDC) systems (e.g., Medidata RAVE or similar); prior involvement in data query management and data cleaning activities preferred
Experience with clinical data review, including safety, efficacy, and/or laboratory data, and familiarity with statistical approaches
Hands-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 stakeholders.
High attention to detail and strong organizational skills
Experience in autoimmune disease, immunology, neurology, or hematology is preferred.
Willingness to travel as needed to support clinical sites, investigator meetings, and scientific conferences.

Benefits

Comp & perks

bonus
benefits
equity participation

ATS Keywords

✓ Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical trial designdata query managementdata cleaningclinical data reviewsafety data analysisefficacy data analysislaboratory data analysisstatistical approachesrisk identificationmitigation strategies

Soft Skills

independent workcollaborative workcommunication skillsattention to detailorganizational skillsability to influence stakeholdersadaptabilityproblem-solvingcritical thinkingtime management

Certifications

PhDPharmDMD