Associate Director, Clinical Development

📋 Description

• Support research activities to expand Revance therapeutics and indications
• Help design clinical studies and develop/revise protocols for regulatory approval
• Execute Phase 1-3 clinical studies and author regulatory documents
• Represent Revance in regulatory meetings and scientific forums
• Collaborate with CROs, internal teams, and KOLs
• Travel as needed to support programs (up to 30%)

🎯 Requirements

• Minimum seven to ten years in design, execution, evaluation of clinical trials (phases 2-4)
• Recent IND and (s)NDA/BLA submission track record
• Experience with physician- or company-sponsored trials
• Deep understanding of regulatory requirements for NDA/BLA submissions
• Active network in Neurology or Physiatry with KOLs and patient groups
• Strong written communication; experience with CROs and academic partners

🎁 Benefits

• Competitive compensation and performance bonus
• Flexible PTO, holidays, parental leave
• Comprehensive health benefits, 401k match, and additional perks