Allergan Assoc Dir, Biostatistics in Irvine, California
Assoc Dir, Biostatistics
Irvine, California, United States at https://agn.referrals.selectminds.com/jobs/5463/other-jobs-matching/location-only
May 22, 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 Associate Director, Biostatistics position will be based in Irvine, CA and will independently lead one or more projects ensuring the proper design, analysis, and presentation of clinical studies while adhering to timelines and departmental quality-control standards. This position interacts with domestic and foreign regulatory agencies for Allergan R&D projects. The position also monitors budgetary and resource needs, and evaluates, hires, and manages CROs and/or contract biostatisticians.
The employee must conduct their work activities in compliance with all relevant laws, regulations, and regulatory guidelines as well as all Allergan policies and procedures.
Main Areas ofResponsibilities
Independently lead one or more projects ensuring the proper design, analysis, and presentation of clinical studies while adhering to timelines and departmental quality-control standards
Interact with domestic and foreign regulatory agencies for Allergan R&D projects.
Monitor budgetary and resource needs, and evaluates, hires, and manages CROs and/or contract biostatisticians.
Assist statistical science process development as needed to improve the efficiency and standardization.
Represent Statistical Science and Programming on cross-functional project teams.
Managed a whole typicalproject(s).
Study level statistician forreasonable complex project from study design to CSR.
1-2 NDAs regulatory experience.
- PhD level with at least 7 yearsof experience OR MS level with 9 years in pharmaceutical statistics.
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.