Note: The job is a remote job and is open to candidates in USA. Revance is a global company developing, producing, and distributing products across aesthetics, skincare, and therapeutics. The Associate Director, Clinical Development will support the expansion of therapeutic products and indications by helping establish program strategies, design clinical studies, develop protocols, and execute Phase 1–3 clinical trials. The role will also contribute to regulatory submissions, scientific communications, investigator engagement, and cross-functional clinical development activities.
Responsibilities
- Develop scientific methods, design clinical studies, and develop and implement clinical protocols
- Gather internal and external feedback on clinical research programs
- Be accountable for study protocols in collaboration with the Biometrics, Clinical Operations, Safety, and Medical Affairs groups
- Represent clinical research through membership on trial teams
- Recruit, guide, and motivate clinical investigators
- Support Data Monitoring Committees and Data Safety Monitoring Boards with presentations
- Author relevant sections of protocols, Clinical Study Reports, investigator brochures, IND/BLA submissions, and other clinical/regulatory/safety documents
- Regularly report to clinical development and scientific leadership
- Ensure study compliance by understanding and applying all relevant SOPs and GCPs
- Present technical information to internal teams; represent Revance externally through publications, presentations at scientific meetings and congresses
- Participate in long range strategic product planning for current and future products
Skills
- Minimum seven to ten years' experience in the design, execution and evaluation of clinical trials, with an emphasis on phases 2-4
- Recent track record of successful IND and (s)NDA/BLA submissions
- Responsibility for physician-sponsored or company-sponsored clinical trials
- In-depth understanding of pharmaceutical regulatory requirements and their impact on development of clinical trials and NDA/BLA submissions
- An active network within Neurology or Physiatry. This will include KOLs, key research centers, patient advocacy groups and a variety of patient care organizations
- Able to write clearly and succinctly in a variety of communication settings. Open, transparent and succinct communication skills
- Experience working with corporate/academic partners and contract research organizations
- MD, DO, PhD, PharmD, or other recognized doctorate-level education
- Ability to travel up to 30%
- Excellent communication skills, both written and oral
- Effective team member with outstanding interpersonal skills
- Ability to develop project strategies and execute project details
- Demonstrated ability to function effectively in a corporate environment while maintaining the highest ethical, regulatory and scientific standards
- Highly developed problem-solving capabilities
- Ability to effectively learn and convey clinical and non-clinical technical information
- Strong presentation and teaching skills
- Ability to work independently and with cross functional teams
- Strong organizational and time management skills, with the ability to manage multiple complex projects
- Strong data analysis capabilities
Benefits
- Annual performance bonus
- Flexible PTO (12 days' PTO)
- Holidays
- Parental leave
- Generous healthcare benefits
- HSA match
- 401k match
- Employer-paid life insurance
- Employer-paid disability insurance
- Pet insurance
- Wellness discounts
Company Overview