Apogee Therapeutics - Research and Development, Remote work

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 ...

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...

Lead late-phase tech transfer and purification process development for protein biologics at a CDMO. This director role requires a PhD and 10+ years of GMP biologics experience from development through commercialization. You will provide technical leadership, support manufacturing campaigns, and a...

Lead late-phase cell culture development and commercialization for protein biologics. This Director role requires a PhD and 10+ years of experience in biologics manufacturing, CDMO tech transfer, and cGMP. You will provide technical leadership from lab-scale to GMP production, supporting regulato...

Lead late-stage development and commercialization of monoclonal antibodies as an MSAT Associate Director. This role provides technical oversight for Drug Substance manufacturing at CDMOs, from tech transfer to PPQ. Requires a PhD and 7+ years of biologics experience. Enjoy competitive compensatio...

Lead biostatistics for key clinical projects as an Associate Director. This senior role requires 8+ years' experience, including Phase 3 studies and regulatory submissions. You will provide expert statistical leadership from design through analysis. We offer a competitive compensation package and...