Allergan Senior Manager, Clinical Trial in Irvine, California

Senior Manager, Clinical Trial

Irvine, California, United States at

▾ ▸ 1 additional location

Madison, New Jersey, United States

Nov 07, 2018Post Date

184858Requisition #

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.

Position Overview

The Senior Manager, Clinical Trial is responsible for the operational execution of assigned clinical studies. As well as a CTM role, the Snr CTM is likely to be assigned as the Operations Study Lead (OSL) of a global study. They may also be assigned a Program Operations Lead (POL) role for a small program.

This position can also act as an Operations Study Lead (OSL) whowill be responsible for all study management aspects of a global clinical study.

Main Areas of Responsibilities

The incumbent ensures the assigned clinical study(ies) is run to time and budget and is completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all Allergan policies and procedures.

The incumbent will be responsible for all regional study management aspects of a clinical study including but not limited to all of the tasks specified below. For all of the regional study activities in a global study, the incumbent will work with the OSL/SnrCTM to ensure correlation of global study activities.

Study Concept, Planning and Strategy Phase

The incumbent is responsible to work with the FACT team for regional study feasibility, the initial assessment of any vendors, supplies planning and the development of study specific documents and timelines as required.

Study Initiation Phase

The incumbent is responsible for: region-specific document development including the informed consent forms; regional investigator meetings;/presentation of materials; the development of regional enrolment initiatives; input any regional specifics to the global study budget via the OSL; planning regional clinical study supplies. They are responsible for obtaining required translations and collecting non-essential documents from site,and ensuring sites are trained in collaboration with the site monitor.

Study Management/Conduct Phase

The incumbent is responsible for: regional financial management; database lock activities; regional study drug management; regional trial master file management; regional study enrolment management (e.g. contingency plan execution); ongoing review of protocol deviations; regional vendor management; and ensuring compliance of adverse event reporting.

Close-Out Phase

The incumbent is responsible for: supporting database lock activities; ensuring all regional documents are filed in the TMF sections appropriately; ensuring all close-out activities are completed; ensuring study documentation is properly archived when the study is considered completed.


  • Proven success in clinical trial management

  • Early and late phase, and/or therapy area experience is an advantage

  • Good Clinical Practices, ICH guidelines, PhRMA code, CFR Guidelines, clinical research ethics, HIPAA and patient privacy laws (plus applicable local regulations, when country-based),

  • Knowledge of concepts of clinical research and drug development, andGeneral therapeutic area education and training


  • Science Degree (or health-related field) or higher degree

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.