Jobs at Atrium Therapeutics, Inc.

Manage end-to-end clinical trial material supply and logistics for biopharmaceutical programs. Responsibilities include supply forecasting, IRT/RTSM oversight, packaging and labeling, depot and vendor management, distribution, cold-chain shipping, import/export compliance, and temperature excursion investigations. The role coordinates with clinical, quality, regulatory, technical operations, CMOs, CROs, and logistics partners to ensure compliant, uninterrupted drug supply and inspection-ready documentation.

Lead operational execution of outsourced nonclinical programs (GLP and non-GLP toxicology and PK) at CROs, manage timelines, budgets, vendor qualification/contracting, and departmental financial stewardship. Coordinate cross-functional stakeholders, support study data/report management and regulatory documentation, and perform on-site and remote CRO monitoring to advance programs to IND and beyond.

Execute in vivo rodent studies to characterize Antibody Oligonucleotide Conjugates for cardiac programs, with primary emphasis on mouse echocardiography. Develop and characterize cardiac disease models, perform ECGs, dosing (IV/SC/IP/RO/IM), blood/tissue collection, necropsy, microdissection, sample handling, data analysis, and present results to multidisciplinary teams.