Clinical Affairs Scientist

Role: Clinical Affairs Scientist supporting clinical evidence generation for companion diagnostics in oncology within Agilent’s medical diagnostic field. Responsibilities: design and oversee clinical trial protocols, contribute to regulatory submissions, author scientific reports and manuscripts, develop databases and data collection tools, ensure study quality and compliance, and provide scientific oversight of marketing materials. Collaborate with cross-functional teams including R&D, Regulatory, and Quality, and serve as a clinical science expert in internal and external meetings. Qualifications: Master’s degree or higher (Ph.D., Pharm.D., M.D.) in biomedical sciences, with 4+ years’ experience in IVD product development, clinical research, or medical writing, especially in pharma or medical devices. Skills: strong scientific and medical writing, familiarity with clinical trial design, biostatistics, GxP, and regulatory standards, with experience working with external partners and regulatory agencies like the FDA. Preferred: knowledge in oncology, immunology, or pathology. Work setup: full-time, remote option, no travel required.