Cabaletta Bio Inc - United States, IT - Administration

Clinical Sample Manager needed to coordinate daily sample activities for cell therapy trials in the US. Requires 5+ years in clinical sample management, GCP/GLP/IATA knowledge, and LIMS proficiency. You will ensure accurate tracking, chain of custody, and compliance across labs and vendors. Benef...

Senior Director, Field Medical Affairs Team Lead sought to build and execute field medical strategy for rese-cel in myositis and autoimmune diseases. This role requires an advanced degree (PharmD, PhD, MD, DO), 10+ years in pharma/biotech, and 8+ years as an MSL with 3-5 years leading cell therap...

Lead our GxP audit program as an Audit Director in Philadelphia. You will develop strategy, oversee internal/external audits, and ensure compliance with global regulations (FDA, EMA). Mentor a team and drive quality in a fast-paced cell therapy environment. Competitive benefits include health, re...

Lead IT strategy and infrastructure for a biotech leader in Philadelphia. This executive role requires 10+ years of leadership, with deep expertise in GxP, cloud platforms, and cell therapy commercialization. Build and scale secure, compliant systems while enjoying competitive health, retirement,...

Lead clinical development for innovative cell therapies in autoimmune diseases at Cabaletta Bio. This hands-on Senior Medical Director role in Philadelphia requires an MD/PhD with 7+ years in biotech/pharma clinical trials. Provide medical oversight from early to late-stage studies, collaborating...

Lead regulatory strategy for a pivotal cell therapy program from clinical trials to BLA/MAA submission. Utilize your 5+ years of biopharma regulatory experience, including direct BLA expertise, to guide cross-functional teams and engage with global health authorities. This Philadelphia-based role...