Apogee Therapeutics - United States, Remote work

Lead our GMP raw materials QC testing program and support drug substance analytical activities as a key liaison. This role requires 10+ years of biotech QC experience, deep expertise in GMP quality systems, and biologics analytical testing. We offer competitive compensation, equity opportunities,...

Lead IT Infrastructure Operations at a fast-growing, cloud-first biotech. This newly created role requires 7+ years of experience, expertise in Azure/M365/IAM, and managing MSP partnerships. Drive excellence, support scientific breakthroughs, and enjoy competitive compensation with equity in a co...

Seeking an experienced biotech contracts professional to join our Legal Department in the United States. You will draft, negotiate, and manage a high volume of clinical and corporate agreements, including CTAs and MSAs. This role requires 6+ years of life sciences industry experience and offers a...

Lead global clinical trial programs (Phases II-III) in this fully remote Executive Director role. You will provide strategic operational management, driving execution with 20+ years of clinical research experience. This position offers competitive compensation, equity opportunities, and a chance ...

Lead our late-stage biomarker development for inflammatory and immune diseases, including atopic dermatitis and asthma. This senior VP role requires a PhD/MD with 15+ years of leadership experience, focusing on Phase 3 trials and BLA submissions. We offer a competitive compensation package and a ...

Seeking a remote Logistics & Inventory Manager to oversee GMP/non-GMP clinical supply chains. You will act as a trade compliance expert and Importer of Record, ensuring timely global material flow. The role requires 5+ years' experience, IoR hands-on practice, and knowledge of international regul...

Join our team as an Associate Director of Clinical Quality Assurance (CQA). This key role requires 8-10 years of biopharma QA experience, including 6 years in GCP auditing. You will ensure regulatory compliance, develop audit plans, and foster a quality culture. We offer a dynamic environment wit...

Lead global Phase II-III clinical trials from planning to completion in this Associate Director role. You will ensure GCP compliance, manage CRO partnerships, and oversee study execution to meet quality and timeline goals. This US-based position requires 8+ years of clinical research experience, ...

Lead late-phase and commercial drug product development for biologics, focusing on prefilled syringes and combination products. Utilize your 10+ years of industry expertise to oversee tech transfer, GMP manufacturing at CDMOs, and ensure robust clinical/commercial supply. Provide strategic techni...

Lead analytical quality control efforts for a complex biologics pipeline in this Associate Director role. You will provide technical oversight for QC testing, method lifecycle management, and regulatory submissions, ensuring cGMP compliance. This hands-on position requires 7+ years of experience ...

Join Apogee's Technical Operations team as a Senior CMC Project Manager. You will manage CMC documentation, lead SharePoint/Veeva migrations, and provide project support for biologics programs. The role requires 5+ years in biotech/pharma with strong CMC, Smartsheet, and timeline management exper...

Lead clinical execution and medical monitoring for dermatology studies as a Medical Director. This role requires an MD with dermatology and clinical development experience in Immunology & Inflammation. You will drive protocol development and study execution for Phase 2/3 trials in the United Stat...