Manager, Aesthetics Clinical Development

Job Description 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. To build all necessary data and information needed in preparing internal documents and scientific reports related to clinical trials and to keep multiple reports moving forward simultaneously through multi‑tasking. Prepare scientific reports and presentations related to clinical trials using available software and templates, review and contribute to clinical protocols, and 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 the study development by applying the most current electronic document conventions and processes consistently to ensure scientific integrity of all processes. Receive and complete tasks and assignments from function, therapeutic area MD or scientific staff within timelines with minimal supervision and maximize individual, function, or therapeutic area and team productivity. Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management. Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded or unblinded PK, safety, and efficacy reviews, ensuring the scientific integrity of all processes. Perform literature and competitive intelligence searches to recognize and resolve scientific and technical problems by applying the most current electronic document conventions consistently and accurately. Provide or present key clinical study information to function, therapeutic area, and management. May lead teams within therapeutic area and supervise exempt and or non‑exempt direct reports and mentor function or therapeutic area personnel. The position is based onsite in Irvine, CA. Qualifications Bachelor’s or Master’s degree in a science related field with 11 or more years of experience in the pharmaceutical industry or Pharm‑D or PhD with 1 or more years of experience. Ability to understand more complex clinical study principles. Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports, and create presentations, posters, and manuscripts. Experience in team, drug development, and scientific project leadership or related. Experience supporting clinical research, drug development, and or function or therapeutic area operations. Proven record of successful projects. Experience in multi‑faceted, broad‑based multiple functions or therapeutic areas 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. Attention to detail and ability to produce work of the highest quality. Good oral and written communication skills. Benefits Comprehensive benefits package including paid time off (vacation, holidays, sick), medical, dental, and vision insurance, and 401(k) to eligible employees. Eligibility to participate in short‑term incentive programs. Eligibility to participate in long‑term incentive programs. Equal Opportunity AbbVie 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. US & Puerto Rico only - to learn more. US & Puerto Rico applicants seeking a reasonable accommodation may consult our accommodations policy. #J-18808-Ljbffr Allergan