Clinical Trial Manager
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values, Stay True to Why, Collaborate to Accelerate, Lead with Clarity, Boldly Innovative, and Own the Outcome, we are committed to transforming the future of treatment for autoimmune disease. Join us at the forefront of cell therapy innovation and help redefine what’s possible.
The Clinical Trial Manager (CTM) will support the operational execution of cell therapy clinical trials, with a primary focus on vendor management, including central laboratory oversight. This role is responsible for ensuring vendors deliver high-quality, timely services aligned with study timelines, budgets, and regulatory requirements.
This position requires strong vendor oversight capabilities and hands-on clinical operations experience, particularly in managing central labs and other external partners supporting complex cell therapy trials.
Title: Clinical Trial Manager
Location: Remote
Reports to: Executive Director, Clinical Operations
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Responsibilities
Serve as the primary contact for assigned vendors
Participate in vendor selection activities (as needed)
Develop and track study timelines, budgets, forecasts, and key performance indicators.
Assist in day-to-day operational execution of assigned clinical trials from startup through close-out.
Oversee site feasibility, selection, contracting, start‐up (site initiation visits, training, enrollment & retention strategies) and close‐out activities.
Conduct Monitoring Oversight Visits (as needed)
Support delivery of study milestones in alignment with program objectives.
Lead vendor oversight through:
Governance structures (e.g., recurring vendor meetings, KPIs, performance dashboards)
Issue identification, escalation, and resolution
Oversight of deliverables, timelines, and quality
Ensure central lab operational readiness, including:
Lab manual review and site training coordination
Sample collection, processing, and shipment workflows
Data transfer specifications and reconciliation with data management systems
Partner closely with vendors to ensure timely, accurate data delivery.
Review and approve vendor deliverables, invoices, and change orders; track spend vs. budget.
Partner with cross-functional teams (Clinical Ops, Data Management, Biostatistics, Regulatory, Safety, Manufacturing, Supply Chain, Quality) to ensure aligned study execution.
Communicate vendor performance and escalate risks/issues to leadership as needed.
Identify and track risks related to vendor performance, lab data quality, logistics, and timelines.
Collaborate cross-functionally to implement mitigation plans.
Contribute to development/review of study documents (protocols, ICFs, CRFs, monitoring plans, lab manuals, data review plans).
Support process improvements, particularly in vendor governance and central lab operations.
Contribute to SOP development and best practices within Clinical Operations.
Qualifications
B.S. degree with 4+ years of clinical operations experience in biotech or pharmaceutical industry.
Strong vendor management experience required, including oversight of central laboratories.
Strong understanding of managing clinical trials from startup through close-out.
Exposure to cell therapy, CAR-T, or advanced biologics preferred.
Working knowledge of ICH-GCP, FDA, and EMA regulations.
Strong organizational, communication, and problem-solving skills.
Ability to manage multiple priorities and work with moderate supervision.
Experience in a biotech or startup environment preferred.
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The national base salary range for this position is $135K-$155K annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data. This position is also eligible for bonus, benefits, and participation in the company's stock plan.
Apply To This Job
The Clinical Trial Manager (CTM) will support the operational execution of cell therapy clinical trials, with a primary focus on vendor management, including central laboratory oversight. This role is responsible for ensuring vendors deliver high-quality, timely services aligned with study timelines, budgets, and regulatory requirements.
This position requires strong vendor oversight capabilities and hands-on clinical operations experience, particularly in managing central labs and other external partners supporting complex cell therapy trials.
Title: Clinical Trial Manager
Location: Remote
Reports to: Executive Director, Clinical Operations
n
Responsibilities
Serve as the primary contact for assigned vendors
Participate in vendor selection activities (as needed)
Develop and track study timelines, budgets, forecasts, and key performance indicators.
Assist in day-to-day operational execution of assigned clinical trials from startup through close-out.
Oversee site feasibility, selection, contracting, start‐up (site initiation visits, training, enrollment & retention strategies) and close‐out activities.
Conduct Monitoring Oversight Visits (as needed)
Support delivery of study milestones in alignment with program objectives.
Lead vendor oversight through:
Governance structures (e.g., recurring vendor meetings, KPIs, performance dashboards)
Issue identification, escalation, and resolution
Oversight of deliverables, timelines, and quality
Ensure central lab operational readiness, including:
Lab manual review and site training coordination
Sample collection, processing, and shipment workflows
Data transfer specifications and reconciliation with data management systems
Partner closely with vendors to ensure timely, accurate data delivery.
Review and approve vendor deliverables, invoices, and change orders; track spend vs. budget.
Partner with cross-functional teams (Clinical Ops, Data Management, Biostatistics, Regulatory, Safety, Manufacturing, Supply Chain, Quality) to ensure aligned study execution.
Communicate vendor performance and escalate risks/issues to leadership as needed.
Identify and track risks related to vendor performance, lab data quality, logistics, and timelines.
Collaborate cross-functionally to implement mitigation plans.
Contribute to development/review of study documents (protocols, ICFs, CRFs, monitoring plans, lab manuals, data review plans).
Support process improvements, particularly in vendor governance and central lab operations.
Contribute to SOP development and best practices within Clinical Operations.
Qualifications
B.S. degree with 4+ years of clinical operations experience in biotech or pharmaceutical industry.
Strong vendor management experience required, including oversight of central laboratories.
Strong understanding of managing clinical trials from startup through close-out.
Exposure to cell therapy, CAR-T, or advanced biologics preferred.
Working knowledge of ICH-GCP, FDA, and EMA regulations.
Strong organizational, communication, and problem-solving skills.
Ability to manage multiple priorities and work with moderate supervision.
Experience in a biotech or startup environment preferred.
n
The national base salary range for this position is $135K-$155K annually. This salary range is an estimate of what we reasonably expect to pay for this position, and the actual salary may vary based on various factors that may include but are not limited to quality and length of experience, education, geographic location and alignment with market data. This position is also eligible for bonus, benefits, and participation in the company's stock plan.
Apply To This Job