• Serve as a primary Sponsor medical representative for assigned clinical trial, working closely with the CRO medical monitor and cross-functional partners, and pharmacovigilance on study execution including but not limited to safety reporting, escalation for medical issues, development and execution of the Medical Monitoring Plan • Contribute to protocol development, study documents, operational plans, and other relevant documents for individual studies • Support all the start-up activities related to the assigned Dermatology clinical study including investigator training, vendor discussions, cross-functional team reviews • Oversee day-to-day clinical and medical execution of studies including direct medical review of eligibility, safety events, and clinical data • Work closely with cross-functional colleagues, including, but not limited to regulatory, biostatistics, and data management, to ensure timely and flawless execution of clinical plan and study milestones in alignment with business goals • Partner with clinical operations on site selection, recruitment, site relationship management and CRO management • Partner with medical affairs to build and maintain strong relationships with PIs by participating in KOL interactions and scientific engagement activities