Allergan Manager, Compliance in California
California, United States at https://agn.referrals.selectminds.com/jobs/7413/other-jobs-matching/location-only
Dec 03, 2018Post Date
Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world.
Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day.
Allergan is a company that will inspire you to aim high with your ambition. Where you can build bridges all over the world. Where you can power ideas that drive change. And where you will act fast and drive results for customers and patients. Power your future & join our bold team.
the Manager partners with R&D organization to understand business priorities and provide compliance support on the business’s strategy, tactics and operations with a primary focus on interactions with healthcare professionals and effective execution of R&D initiatives.
Main Areas of Responsibilities
Provide timely and practical advice and support for questions and concerns regarding compliant activities
Provide support of key business operations functions and Centers of Excellence
Partner with members from Medical Affairs, Clinical Development, Drug Development, Clinical Operations, Legal, and Business Operations departments for compliance-related activities
Develop and deliver regular and ongoing training and education to the R&D organization
Provide data analytics and reporting related to monitoring findings and other compliance observations to internal stakeholders as well as external regulators
Manage and maintain database of compliance observations
Assist in compliance monitoring and investigations as needed
4-5 years of experience in Compliance or Pharmaceutical / Device Research and Development, with 2-3 years of experience in the pharmaceutical or medical device industry preferred
Prior experience in business/customer facing role required
Prior experience managing projects
Collaboration: Partner with multiple stakeholders such as Medical Affairs, Clinical Development, Legal, Regulatory and HR in the development of initiatives related to the business goals
Training: Train business partners on compliance guidelines, policies and best practices related to their specific business
Guidance: Provide regular guidance to the business regarding the Global Compliance Program
Reporting: Provide insights to business partners based on compliance data analysis
Requires strong leadership and influencing skills to manage complex projects
Responsible to implement and maintain activities across multiple therapeutic areas
Serves as advisor to client and project manages complex, revenue generating business
Awareness of federal fraud and abuse laws and guidance, including the ACCME guidelines, the Office of Inspector General reports, and the Food, Drug and Cosmetic Act and an understanding of the roles and authority of government agencies and industry partners including FDA, OIG, PhRMA and AdvaMed Education
Bachelor’s degree required
Equal Employment Opportunity Employer
Allergan is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected status.