Kyverna Therapeutics

Senior Specialist, Quality Assurance Operations (Contract)

Senior Specialist, Quality Assurance Operations

Bachelor's in life sciences; 6+ years QA in biotech/pharma/cell therapy; strong QA ops, batch records, regulatory compliance, cross-functional collaboration.

Specialist, Document Management & Training (Contract)

Specialist, Document Management & Training

Support document control and training systems in GMP environment; manage lifecycles and training compliance; generate metrics.

Sr. Clinical Research Scientist

Clinical Research Scientist

PhD/MD/PharmD with 2+ years in biotech/pharma clinical research; strong GCP knowledge; independent, collaborative; EDC experience; autoimmune focus preferred.

Sr. Medical Director, Clinical Development

Medical Director

MD/DO or MD-PhD with 7+ years in clinical research; late-stage trial experience; strong GC/ICH knowledge; leadership in cross-functional settings.

Clinical Trial Manager

4+ years clinical operations in biotech/pharma; strong vendor management incl central labs; trial management from startup to close-out; exposure to cell therapy; ICH-GCP/FDA/EMA knowledge; strong organization and communication; startup experience preferred.

Publications & Conferences Manager  (Consulting position)

Publications & Conferences Manager

Bachelor’s in life sciences; 4+ years in medical/scientific publications or medical affairs; pharma/biotech experience; strong PM; excellent writing; CMPP/CMP a plus.

IT Validation Engineer

Bachelor’s degree; 6+ years IT validation in regulated environments; CSV/CSA expertise; GxP, 21 CFR Part 11 experience; strong documentation; cross-functional collaboration; preferred eQMS/regulatory apps.

Sr. Contracts Counsel - Clinical

Contracts Counsel

JD with regulatory law experience; Bar admission; 8+ years in life sciences contract work; in-house experience preferred; strong negotiation and drafting skills; familiar with contract management systems (Ironclad).

Kyverna

Sr. Manager, GxP Auditor (GCP & GMP)

GxP Auditor

ASQ CQA; BA/BS in biological sciences or related field; 10+ years pharma/biotech; 5+ years GMP/GCP/GVP auditing; knowledge of GMP, GCP, GLP; leadership; travel up to 25%; experience with eQMS and clinical systems

Executive Director, Regulatory Affairs

15+ years regulatory affairs in pharma/biotech with advanced therapies; leadership in regulatory strategy, global submissions, labeling, and health authority engagements.

Sr. Director, Process Development

PhD preferred; 15+ years in biotech/pharma; CAR-T/process development/tech transfer; regulatory and cGMP knowledge.

Executive Director, Strategic Sourcing and Supply Chain

15+ years in pharmaceutical/biopharmaceutical ops; 5+ years leading sourcing or supply chain; direct cell therapy experience; bachelor's in life sciences; MBA or advanced degree preferred; strong leadership and cross-functional collaboration.

Sr. Scientific Advisor CAR T Technologies

Scientific Advisor

PhD in immunology or related field; 10+ years in immunology/drug discovery; deep CAR T and immune cell engineering expertise; experience with preclinical pharmacology; strong collaboration and communication.

Sr. Manager / Assoc. Director, Forecasting & Insights

Forecasting & Insights

8+ years in forecasting/analytics in biopharma; strong leadership; launch planning experience; advanced analytics and scenario modeling.

Sr. Clinical Trial Manager

7+ years clinical operations experience in biotech/pharma; proven cell therapy/CAR-T trials; strong leadership and cross-functional coordination; knowledge of GCP and regulatory requirements.

Director of Training, Global Medical Affairs

Director of Training

Advanced degree; 10+ years biotech/pharma; 5+ years Medical Affairs leadership; cell/gene therapy experience; regulatory/compliance knowledge; strong cross-functional leadership.

Senior Mgr, IT GxP Business Partner

IT GxP Business Partner

Lead GxP IT strategy, implementation, and compliance for R&D/Clinical/Commercial systems; 10+ yrs tech/biotech exp; strong SQL/Power BI; regulatory knowledge.

Sr. Director, Marketing Promotions

Senior leadership for global promotional strategy; 12+ years in pharma marketing promotions; launch experience preferred; cross-functional collaboration; strong regulatory knowledge.

Sr. Director, Business Development

Lead BD, partnerships, licensing and collaborations; 10+ years in biotech; advanced degree; strong negotiation and leadership; cell therapy/autoimmune experience preferred.

Executive Director, Head of Cellular Therapy Operations

Senior biopharma operations leader with 15+ years experience; 5+ years in senior leadership; experience with CAR-T/cellular therapies; strong cross-functional leadership and regulatory/compliance expertise.

Title	Location	Date
Senior Specialist, Quality Assurance Operations (Contract) Contract, Temporary · $114K-$135K/yr · 6+ YOE Emeryville, California, United States · Hybrid	Emeryville, California, United States Hybrid	May 1, 2026
Specialist, Document Management & Training (Contract) Contract · $104K-$125K/yr · 2+ YOE United States · Remote	United States Remote	May 1, 2026
Sr. Clinical Research Scientist Full Time · $140K-$160K · 2+ YOE United States · Remote	United States Remote	May 1, 2026
Sr. Medical Director, Clinical Development Full Time · $330K-$370K · 7+ YOE United States · Remote	United States Remote	Apr 30, 2026
Clinical Trial Manager Full Time · $135K-$155K · 4+ YOE United States · Remote	United States Remote	Apr 24, 2026
Publications & Conferences Manager (Consulting position) Contract, Temporary · $146K-$187K/yr · 4+ YOE United States · Remote	United States Remote	Apr 24, 2026
IT Validation Engineer Full Time · $130K-$145K · 6+ YOE United States · Remote	United States Remote	Apr 22, 2026
Sr. Contracts Counsel - Clinical Full Time · $200K-$235K · 8+ YOE United States · Remote	United States Remote	Apr 21, 2026
Sr. Manager, GxP Auditor (GCP & GMP) Full Time · $155K-$180K · 10+ YOE United States · Remote	United States Remote	Apr 17, 2026
Executive Director, Regulatory Affairs Full Time · $270K-$300K · 15+ YOE United States · Remote	United States Remote	Apr 16, 2026
Sr. Director, Process Development Full Time · $250K-$275K · 15+ YOE Emeryville, California, United States · Hybrid	Emeryville, California, United States Hybrid	Apr 7, 2026
Executive Director, Strategic Sourcing and Supply Chain Full Time · $250K-$290K · 15+ YOE United States · Remote	United States Remote	Apr 1, 2026
Sr. Scientific Advisor CAR T Technologies Contract · 10+ YOE United States · Remote	United States Remote	Mar 20, 2026
Sr. Manager / Assoc. Director, Forecasting & Insights Full Time · $160K-$200K · 8+ YOE Emeryville or United States · Hybrid	Emeryville or United States Hybrid	Mar 18, 2026
Sr. Clinical Trial Manager Full Time · $155K-$180K · 7+ YOE United States · Remote	United States Remote	Mar 13, 2026
Director of Training, Global Medical Affairs Full Time · $210K-$245K · 10+ YOE United States · Remote	United States Remote	Mar 12, 2026
Senior Mgr, IT GxP Business Partner Full Time · $150K-$170K · 10+ YOE Emeryville or United States · Hybrid	Emeryville or United States Hybrid	Mar 6, 2026
Sr. Director, Marketing Promotions Full Time · $260K-$300K · 12+ YOE Emeryville or West Coast Remote · Hybrid	Emeryville or West Coast Remote Hybrid	Mar 5, 2026
Sr. Director, Business Development Full Time · $260K-$290K · 10+ YOE United States · Remote	United States Remote	Feb 11, 2026
Executive Director, Head of Cellular Therapy Operations Full Time · $275K-$305K · 15+ YOE United States · Remote	United States Remote	Jan 22, 2026

Activities	cell therapy developmentclinical drug trialsautoimmune disease researchbiopharmaceutical manufacturingT-cell engineering
Headquarters	US
Industries	BiotechnologyPharmaceuticals
Name	Kyverna Therapeutics
Employees	153
Type	Public
Tagline	Developing cell therapies for patients with autoimmune diseases.
Founded	2,018
Website	kyvernatx.com
Stock Exchange	NASDAQ
Stock Symbol	KYTX

Kyverna Therapeutics

About Kyverna Therapeutics