State Licensed Preclinical Manager

Key Responsibilities: Own the operational health of concurrent preclinical programs, setting timelines and synchronizing studies and stakeholders Coordinate planning and execution of preclinical studies, managing logistics, documentation, and deliverable tracking Manage relationships and project execution with CROs and external partners, ensuring adherence to budgets and timelinesRequired QualificationsDegree in a relevant scientific, biomedical, engineering, or clinical field; clinical/medical background with an active license preferred 3-5+ years of experience in preclinical/clinical research, study coordination, or program management in a regulated environment Proven ability to manage multiple concurrent projects and maintain detailed timelines and trackers Working knowledge of preclinical science and study conduct, including GLP and ISO 10993 standards Hands-on experience in image-guided, interventional, or surgical procedures preferred