Senior/Principal Scientist, DMPK

Responsibilities: DMPK representative supporting project decisions from discovery through clinical stages Design and interpret ADME, PK, and PK/PD studies from routine SAR to mechanistic insights working with external partners Drive DMPK design strategy in close collaboration with Medicinal Chemistry Perform human PK and dose projections, supporting the progression of lead compounds through the screening cascade Author DMPK sections of regulatory documents and respond to queries Work collaboratively with the Senior Director of DMPK to design the overall ADME/DMPK strategy for the company Cross-Functional Collaboration: Work with in vivo pharmacology to interpret exposure–efficacy data and guide compound progression Contribute to safety and toxicology strategy by ensuring compounds meet advancement criteria Collaborate cross functionally and within matrixed environment to advance projects to required milestones External Collaboration Interface with external ADME/DMPK CRO partners to support compound screening and optimization Contribute to experimental planning, data review, and milestone tracking with vendors Ensure high standards of data integrity, documentation, and reproducibility Program Contribution & Scientific Communication Present program data and recommendations at internal governance meetings Provide scientific input into portfolio discussions from an ADME/PK perspective Thorough, meticulous, and detail-focused approach to data handling and documentation Contribute to a collaborative, high-rigor company culture.

Required Skills & Qualifications: PhD in Pharmacokinetics, Pharmaceutics, or related field with a minimum of 3 years of industry experience 3+ years as a small molecule DMPK project representative/lead on cross functional project teams Experience with human PK and dose projections Interest in both discovery and development stage DMPKSome experience with PK/PD modeling and simulation Clear and effective communicator Collaborative mindset, creativity, “can do attitude” and adaptability in a nimble, entrepreneurial biotech environment Legally authorized to work in the US via US citizenship or residency

Preferred: Experience authoring regulatory documents a plus but not required Interest or experience in supporting PBPK outsourcing Expertise in supervising regulated bioanalysis About Axonis Therapeutics: Axonis Therapeutics is a Boston-based, neuro-focused biotechnology company developing a portfolio of first- and best-in-class medicines targeting KCC2, a genetically validated critical mediator of inhibition within the brain. Axonis has brought together a collaborative, creative and determined team of world-leading experts in neuroscience and drug development to discover and develop novel treatments for epilepsy, pain and other neurological disorders. With its proprietary KCC2 discovery engine based on breakthrough science from Boston Children’s Hospital, Harvard and Laval University, Axonis is poised to make a real difference for patients, their families, and the global healthcare system. EEOC Statement: Axonis believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. In addition, Axonis will provide reasonable accommodations for qualified individuals with disabilities.