Associate Director, Aesthetics Clinical Development
$141,500–$268,500 year
HybridIrvine, California, United States
Job Summary
Design, direct, and execute clinical trials and research activities supporting the overall Product Development Plan, ensuring adherence to regulatory requirements and scientific integrity. Lead cross-functional sub-teams to generate, deliver, and interpret high-quality clinical data for safety and efficacy reviews, while overseeing study enrollment, timelines, and protocol deviations. Provide medical direction to project teams, coordinate external expert engagement, and represent AbbVie at investigator and scientific association meetings. Drive research projects to completion resulting in high-quality publications and contribute to the development and execution of the Clinical Development Plan.
Required Qualifications
- Clinical Development experience
- 7+ years of experience
- Knowledge of regulatory requirements governing clinical trials
- Experience in the design and successful execution of registration-track protocols leading to regulatory submission
Desired Qualifications
- Advanced education (e.g., MD, DO, PhD, PharmD, or MA with relevant experience)
- Experience in the successful development of novel medical devices in Aesthetics with similar product profiles as those in development by AbbVie
- Direct experience with regulatory bodies (US and Global)
- Proven ability to collaborate effectively in a cross-functional setting
- Excellent oral and written English communication skills
- Demonstrable evidence of being a motivated and successful self-starter
- Experience in international markets
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