Associate Director, Clinical Development

Role: Associate Director, Clinical Development supporting research and expansion of Revance's therapeutic products, with focus on securing regulatory approval for indications beyond current approvals. Responsibilities: develop clinical strategies, design and implement Phase 1-3 studies, author regulatory documents, and serve as internal scientific partner. Represent the company in external meetings, liaise with KOLs, and collaborate with clinical operations and CROs. Requirements: MD, DO, PhD, PharmD or equivalent; 7-10 years in clinical trial design, execution, and evaluation, with recent success in IND and NDA/BLA submissions, particularly in neurology or physiatry. HighValue: experience in neurology-focused therapeutics, regulatory submissions, and Phase 1-3 development, with strong network within relevant medical communities. WorkSetup: travel up to 30%. The role demands excellent communication, team collaboration, strategic planning, and adherence to GxP and regulatory standards.