Kezar Life Sciences is combining courage, conviction and cutting-edge science to develop breakthrough treatments for immune-mediated and oncologic disorders helping people overcome their disease and live a better life.
Team spirit and strong bonds are at the heart of who we are, and we’re always looking for equally dynamic and motivated individuals to join our team.
Are you interested in helping us create victories for patients most in need? Browse our open positions and apply for one today.
Kezar Life Sciences (NASDAQ: KZR), a clinical stage biopharmaceutical, is seeking a motivated Scientist 1 to join our Pharmaceutical Development team. The purpose of this position is to develop preclinical and clinical formulations, and the analytical methods to characterize them, in support of our small molecule immunology and oncology programs. The successful candidate will be part of a dynamic, interdisciplinary team requiring a high degree of creativity and initiative. This is an exciting time to help drive the development of novel therapies for unmet needs in multiple indications.
Are you interested in this position?
For more information, please contact us at HR@kezarbio.comScientist : Apply Now
Kezar Life Sciences (NASDAQ: KZR), a clinical stage biopharmaceutical company, is seeking an experienced, dynamic, and highly motivated Senior Manager/Associate Director of Regulatory Affairs who will provide support to the Senior Director, RA. Kezar is focused on small molecule drug development and discovery to target autoimmune/inflammatory disorders (lupus/lupus
nephritis, dermatomyositis/polymyositis, autoimmune cytopenia) and oncology based on the biology of protein homeostasis. Our lead compound, KZR-616 (a selective inhibitor of the immunoproteasome), is in Phase 2 clinical trials, and we are planning for expansion into other indications. We have multiple drug discovery programs targeting protein secretion, and one drug candidate (KZR-261) that is completing IND-enabling activities with plans to conduct the first-in-human oncology study starting in 2021. This is an exciting time to help drive the development of novel therapies for unmet needs in multiple indications.
This position will be responsible for assisting with regulatory strategy, contributing to Agency meetings, and management of worldwide regulatory submissions and responses. In this role, emphasis will be on proper strategic and operational planning, collaboration with development
team members, and execution on all aspects of regulatory affairs.
Essential Duties and Responsibilities:
For more information, please contact us at HR@kezarbio.comSenior Manager/Associate Director: Apply Now