Kyverna1mo ago

Clinical Trial Manager / Sr. Clinical Trial Manager

RemoteRemoteFull Timesenior

OtherHealthcareClinical Trial Manager

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Overview

Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by our core values,

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OtherHealthcareClinical 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 / Sr. Clinical Trial Manager will lead the operational delivery of one or more cell therapy clinical trials from study design through close-out. CTM / Sr. CTM will be accountable for timelines, budget, quality, vendor & CRO oversight, and cross-functional coordination for the assigned studies. Given the complexity of cell therapies (manufacturing, specialized logistics, regulatory, unique site burden), this role requires deep knowledge of clinical operations plus specific experience in cellular therapies or advanced biologics.

Title: Clinical Trial Manager / Sr. Clinical Trial Manager

Location: Remote

Reports to: Sr. Director, Clinical Operations

Lead and manage the day-to-day operational execution of assigned cell therapy trials: study startup, site activation, enrollment, monitoring, close-out.
Develop and manage study timelines, budgets, forecasts, and related operational metrics.
Partner with external vendors / CROs / service providers (monitoring, labs, imaging, manufacturing/supply chain for cell product) to ensure high quality and timely deliverables.
Serve as the primary cross-functional operational contact for study teams (clinical operations, data management, biostatistics, regulatory, safety/pharmacovigilance, manufacturing, supply chain, medical affairs, quality).
Ensure compliance with regulatory and quality standards (FDA, EMA, ICH-GCP, relevant local regulations) and internal SOPs.
Participate in protocol development and amendments, informed consent form (ICF) review, CRF/data tool development, TMF (Trial Master File) setup & maintenance, monitoring plan, data review plan, drug/cell-product accountability and reconciliation.
Oversee site feasibility, selection, contracting, start‐up (site initiation visits, training, enrollment & retention strategies) and close‐out activities.
Monitor study progress, identify risks/issues (enrollment delays, monitor/vendor performance, budget overruns, data quality issues) and implement mitigation strategies.
Foster effective communication across study teams, escalate issues to senior leadership as needed.
Ensure preparation for audits/inspections, maintain high standards of documentation readiness.
Contribute to lessons-learned and process improvement initiatives, particularly around cell-therapy-specific operational challenges (e.g., chain of identity/chain of custody, logistics of product, unique site training).
Review invoices and track study budget according to the forecast, working closely with finance and clinical business operations.
Develop study documents and tools including study, informed consent forms, project plans, budgets, study templates, and other materials as needed.
Vendor Management – Contribute to or lead cross-program vendor management activities
Contribute to SOP development within the Clinical Operations team

B.S. degree with minimum 5+ years of experience in clinical operations including managing clinical trials in biotech, pharmaceutical.
Strong clinical study conduct experience from start-up through close-out.
Strong leadership, effective decision making, and problem-solving skills required.
Established Cell Therapy /CAR T study experience required.
Working knowledge of relevant GCPs and FDA/EMA regulations.
Knowledgeable of current ICH GCP guidelines and applicable regulations.
Ability to work effectively with minimal supervision and multi-task activities to effectively manage deliverables across all trials.
Experience in small/mid biotechnology environment (startup mindset)
Excellent written and verbal communication skills