Manager, Aesthetics Clinical Development

About the Company

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.

About the Role

At Allergan Aesthetics, an AbbVie 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 role involves building necessary data and information for preparing internal documents and scientific reports related to clinical trials, while keeping multiple reports moving forward simultaneously. The position is based onsite in Irvine, CA.

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using available software and templates.
• Review and contribute to clinical protocols by utilizing expertise to assist in interpretation of data.
• Coordinate advisory meeting agendas, activities, slide decks, and consulting agreements.
• Comply with procedures set forth in relevant IQS documents, study protocols, and other directives issued by management regarding clinical studies.
• Lead study development by applying the most current electronic document conventions and processes to ensure scientific integrity.
• Receive and complete tasks and assignments from function, Therapeutic Area MD, or Scientific Staff within timelines with minimal supervision.
• Maximize individual, functional/therapeutic area, and team productivity.
• Participate in process improvement initiatives and review key decisions impacting project timelines with management.
• Analyze clinical study data, including statistical data, using available software for ongoing blinded/un-blinded PK, safety, and efficacy reviews.
• Perform literature and competitive intelligence searches to recognize and resolve scientific and technical problems.
• Provide and present key clinical study information to function, therapeutic area, and management.
• May lead teams within the therapeutic area, supervise exempt and/or non-exempt direct reports, and mentor personnel.

Qualifications

• Bachelor’s or Master’s degree in a science-related field with 11+ years’ experience in the pharmaceutical industry, or Pharm-D/PhD with 1+ year of experience.
• Ability to understand complex clinical study principles.
• Advanced understanding of technology necessary to analyze clinical study data, generate reports, and create presentations, posters, and manuscripts.
• Experience in team leadership, drug development, and scientific project leadership.
• Experience supporting clinical research, drug development, and/or function/therapeutic area operations.
• Proven record of successful projects.
• Experience in multi-faceted, broad-based functions or clinical functions with in-depth knowledge of clinical study issues.
• Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
• High-quality work production with attention to detail.
• Strong oral and written communication skills.

Benefits

• Comprehensive package including paid time off (vacation, holidays, sick).
• Medical, dental, and vision insurance.
• 401(k) retirement plan.
• Eligibility to participate in short-term and long-term incentive programs.