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

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