Clinical Affairs Scientist

Role: Clinical Affairs Scientist supporting clinical evidence generation for companion diagnostics in oncology within Agilent's global clinical team. Responsibilities: lead study design and execution, develop databases and EDC systems, contribute to validation and analytical studies, ensure clinical data integrity and regulatory compliance, author scientific publications, and support audits. Collaborates with R&D, regulatory, quality, and external pharma partners, providing clinical/scientific oversight. Qualifications: Master's or higher degree (Ph.D., Pharm.D., M.D.) in biomedical sciences; 4+ years in IVD product development, clinical research, or medical writing; familiarity with clinical trial design, biostatistics, and GCP; strong scientific and medical communication skills. Preferred: experience with regulatory agencies like FDA; knowledge in oncology, immunology, or pathology. HighValue: oncology diagnostics, companion diagnostics, clinical trial oversight, regulatory interactions, GxP, medical device/pharma industry. Work Setup: full-time, remote option; no travel required.