Associate Director, Clinical Development
revanceFranklin (TN)
Associate Director, Clinical Development
Posted today
revanceFranklin (TN)
SENIORITY
Manager
About the role
Overview:
In this role you will advance Revance therapeutics by designing and executing Phase 1–3 clinical studies and shaping clinical program strategy. You will collaborate with cross-functional teams to develop protocols, support regulatory submissions, and contribute to scientific communications. You’ll engage with external KOLs, convene with internal stakeholders, and ensure study execution in line with GCP/ SOPs. You’ll also help prepare publications and presentations, representing Revance at regulatory meetings and scientific conferences. This is a high-impact, science-driven position with opportunities to influence product strategy and translational development. Compensation / Benefits competitive base salary annual performance bonus flexible PTO and holidays parental leave healthcare benefits HSA match and 401k match
Responsibilities:
Design clinical studies and protocols; develop and implement protocols Collaborate with Biometrics, Clinical Operations, Safety, and Medical Affairs on study plans Represent clinical research on trial teams and interact with external partners Recruit, guide, and motivate clinical investigators Support Data Monitoring Committees and Data Safety Monitoring Boards with presentations Author protocol sections, Clinical Study Reports, investigator brochures, IND/BLA submissions Ensure study compliance with SOPs and GCPs Present technical information to internal teams and external audiences Engage in long-range strategic product planning for current and future products
Key requirements:
7-10 years’ directly related experience in design, execution, and evaluation of clinical trials (phases 2-4) Experience with IND and (s)NDA/BLA submissions Active network within Neurology or Physiatry (KOLs, centers, patient orgs) Strong communication and writing skills Ability to work with CROs and corporate/academic partners Independent work style with cross-functional collaboration Strong data analysis and problem-solving capabilities Willingness to travel up to 30% excellent written and verbal communication collaboration and teamwork problem-solving clinical trial design regulatory submissions (IND/BLA) GCP/SOP compliance
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