Clinical Affairs Scientist

Role: Clinical Affairs Scientist supporting clinical evidence generation for oncology companion diagnostics within Agilent’s medical diagnostic division. Responsibilities: design and oversee clinical trial protocols, contribute to regulatory submissions, generate scientific content and reports, ensure compliance with quality standards, and provide scientific oversight for marketing materials. Collaborates with pharma partners, R&D, regulatory, QA, and clinical teams; serves as a clinical science SME. Requirements: Master's degree (Ph.D., Pharm.D., M.D.); 4+ years in IVD product development, clinical research, or medical writing, with experience in clinical trial design, biostatistics, and GCP. HighValue: oncology diagnostics, companion diagnostics, clinical trial design, regulatory submission support, biostatistics, scientific writing, cross-functional collaboration, remote work flexibility. WorkSetup: full-time, remote option; no travel expected.