Kymera Therapeutics is a clinical-stage biotechnology company specializing in targeted protein degradation (TPD) to develop innovative medicines for critical health problems. Founded in 2016, Kymera focuses on delivering oral small molecule degraders that address disease targets inaccessible with conventional therapies, offering a new generation of effective treatments. Recognized as one of Boston’s top workplaces, the company is pioneering this cutting-edge approach to improve patient outcomes.
Open Positions
Senior Medical Director, IRF5 Program
MD/PhD with board certification in Rheumatology, Immunology, or related discipline; 4+ years of experience in clinical drug development; strong understanding of translational science, biomarkers, and mechanistic drug development
Scientist II or Senior Scientist, Targeted Proteomics
PhD in Biochemistry, Biology, Chemistry, or Chemical Biology with 2+ years of experience in targeted proteomics or BS/MS with 8+ years of relevant experience
Associate Director or Director, Regulatory Affairs
6+ years of Regulatory Affairs experience, Bachelor's degree in a scientific discipline, excellent understanding and knowledge of global drug development and regulatory principles and practices
Translational Medicine Operations Specialist
2-5 years of experience in laboratory sample logistics and/or clinical trials; Bachelor's degree with science focus; Strong organizational skills and attention to detail
Senior Medical Science Liaison- Dermatology
Advanced scientific degree, minimum 5 years of experience, strong understanding of immunology therapeutic area and clinical development
Graphic Designer
3-5 years of graphic design experience, fluency in Adobe Creative Suite, and experience with scientific data visualization tools
Sr. Medical Science Liaison- West- Respiratory
5+ years of experience in a scientific, clinical, or MSL role within the pharmaceutical or biotech industry. Advanced scientific degree (PharmD, MD, PhD) required. Strong understanding of immunology therapeutic area and clinical development
Director, Process Engineering
Ph.D., M.S., or B.S. in Chemical Engineering, 15+ years of experience in small molecule pharmaceutical process engineering, strong understanding of chemical reaction engineering, unit operation modelling, crystallization, isolation, and purification processes
Research & Development Project Coordinator
3+ years of experience in biotech/pharma, results-driven, excellent communication skills, and experience with Microsoft Project, SharePoint, ThinkCell