• Collaborate with cross-functional teams to develop clinical documents for dermatology-related trials with scientific rigor, such as protocol, investigator brochure, clinical study report, scientific publications/presentations, etc. • Contribute scientific input and implementation into the study design and execution, including but not limited to selection of appropriate endpoints, patient populations, and study methodologies; site selection; investigator meetings; and study initiation activities • Monitor the clinical trials for both quality and safety, ensuring adherence to protocols, timelines, and quality standards • Analyze clinical trial data, interpret results, and provide scientific insights to guide decision-making • Collaborate with data management and biostatistics to develop and validate data collection tools and ensure accurate and timely data capture • Foster relationships with clinical investigators to gather insights, address scientific questions, and promote collaboration • Stay current with scientific literature and advancements in dermatology/immunology and related therapeutic areas • Collaborate with clinical operations, medical affairs, regulatory affairs, biostatistics, and other teams to ensure alignment of clinical strategies with overall program goals