Associate Director, Aesthetics Clinical Development

Job Description

At Allergan Aesthetics, an Abb Vie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more.

With our own research and development team focused on driving innovation in aesthetics, we’re committed to providing the most comprehensive science-based product offerings available.

The Associate Director will provide direction and oversight to the design, planning and execution of research activities including but not limited to clinical trials in Aesthetic Medicine. Participate and lead cross-functional teams to generate, deliver and interpret high quality research and clinical data supporting aesthetic indications and overall asset program strategy. As a clinical development subject matter expert, author, edit and review key section of research protocols, reports and regulatory submissions.

• Based on strong medical and scientific experience, knowledge of compliance and regulatory requirements, Allergan Aesthetics customers, markets, business operations and emerging issues, manage the design and implementation of research protocols for clinical development programs in support of the overall Product Development Plan.
• Oversee project‑related education of investigators, study site personnel and Abb Vie study staff.
• Responsible for understanding and addressing applicable regulatory requirements related to the clinical studies, clinician reported outcomes, patient reported outcomes and global drug development. Specifically in the area of aesthetic development.
• Contribute to the design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers, regulatory submissions and responses and other program documents.
• Contribute to the development of a rigorous, cross‑functionally‑aligned, vetted Integrated Evidence Plans in collaboration with matrix team members.
• Participate in opinion leader interactions related to the disease area(s); partner with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies.
• Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.

The position is based onsite in Irvine, CA.

• Bachelor’s degree in the sciences; advanced degree (e.g., MS, PhD) preferred.
• Ability to provide input and direction to clinical research teams with minimal supervision.
• Strong cross‑functional collaboration and leadership skills in a team‑matrixed environment.
• Demonstrated ability to select, contract and manage vendor, ensuring high‑quality and on‑time deliverables.
• Minimum 7 years of overall work experience or equivalent combination of experience and education.
• Minimum 5 years of clinical/research experience in the pharmaceutical/device industry preferred.
• Knowledge of clinical trial methodology, regulatory and compliance requirements in Aesthetic Medicine.
• Ability to interact externally and internally to support global scientific and business strategy. Must possess excellent oral and written English communication skills.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical, dental, vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short‑term incentive programs.
• This job is eligible to participate our long‑term incentive programs.
Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.