Associate Director, Clinical Scientist, Ophthalmology

Role: Lead clinical scientist responsible for scientific planning, strategy, and execution of Phase 1-4 clinical studies in ophthalmology. Main objectives include overseeing clinical/scientific activities, ensuring protocol compliance, and collaborating with cross-functional teams. Responsibilities encompass protocol execution, medical monitoring, data interpretation, and supporting regulatory document development, with potential team management. Required qualifications include a minimum of 6-8 years in pharmaceutical or clinical drug development within ophthalmology, with degrees in life sciences, PharmD, or PhD preferred. Skills in clinical research, GCP, study design, and scientific communication are essential. High-value specifics: ophthalmology focus, clinical trial phases 1-4, GCP compliance, data interpretation, and cross-functional stakeholder engagement. The role involves 10% travel, hybrid work setting, and reports to the Program Lead.