Associate Director, Clinical Development

Responsibilities

• Develop scientific methods, design clinical studies, and implement clinical protocols
• Author protocols, Clinical Study Reports, investigator brochures, and IND/BLA submissions
• Represent the company in regulatory meetings and scientific conferences
• Recruit and motivate clinical investigators
• Collaborate with Biometrics, Clinical Operations, Safety, and Medical Affairs groups
• Participate in long-range strategic product planning

Requirements

• MD, DO, PhD, PharmD, or other recognized doctorate-level education
• 7-10 years of experience in the design, execution, and evaluation of clinical trials (Phases 2-4)
• Proven track record of successful IND and NDA/BLA submissions
• In-depth understanding of pharmaceutical regulatory requirements
• Active network within Neurology or Physiatry, including KOLs and research centers
• Experience working with corporate/academic partners and CROs

Preferred Qualifications

• Strong data analysis and problem-solving capabilities
• Excellent written and oral communication skills
• Ability to manage multiple complex projects independently and in cross-functional teams

Benefits

• Competitive base salary and annual performance bonus
• Flexible PTO, holidays, and parental leave
• Comprehensive healthcare benefits, HSA match, and 401k match
• Employer-paid life and disability insurance, pet insurance, and wellness discounts

About the Company

Revance is a global company developing, producing, and distributing industry-leading products across aesthetics, skincare, and therapeutics, driven by science-powered innovation.