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Takeda Development Center Americas, Inc
Cambridge
Takeda Development Center Americas, Inc. is seeking a Director, PV Risk Management in Cambridge, MA to provide global strategic leadership and expertise in risk management across therapeutic areas. Up to 5% travel required. Up to 100% remote work allowed from anywhere in the US. Full tim...
Job Source: Takeda Development Center Americas, IncTakeda
Boston, MA, United States
Within Takeda’s Data Sciences Institute, we harness the insight of data and digital to speed the development of new medicines to patients. The Data Sciences Institute (DSI) is primarily focused on getting medicines to patients faster through innovation and efficiencies driven by data and analytics. We nurture a culture that encourages disciplined r
Job Source: TakedaTakeda Pharmaceuticals
Boston
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Source: Takeda PharmaceuticalsScott & Crosby Staffing, Inc.
Boston, MA, United States
Job Description Position: Director of Risk Management Department: Risk Management Schedule: Full Time The Director of Risk Management oversees the operation of the Risk Management and Patient Safety programs and provides guidance to clinical staff. The Director will develop and maintain systems to detect, monitor, prevent, organize, measure inve
Job Source: Scott & Crosby Staffing, Inc.HP Hood LLC
Lynnfield, MA, United States
MA, Lynnfield, HPH Lynnfield, MA 01940, USA Description Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future! At HP Hood LLC, we celebrate our differences. Our diversity of people, backgrounds, experiences, thoughts and perspectives are fostered
Job Source: HP Hood LLCPage Mechanical Group, Inc.
Boston, MA, United States
Position: Director, PV Quality and Alliance Management Department: Pharmacovigilance Reports to: Vice President, Pharmacovigilance Location: Boston or Hybrid Summary: The Director, Pharmacovigilance (PV) Quality and Alliance Management will be responsible for leading PV Quality and alliance management activities in collaboration with internal
Job Source: Page Mechanical Group, Inc.ONO PHARMA USA
Cambridge, MA, United States
To promote proper use by conducting necessary internal and external communication such as consultation with the domestic regulatory authority so that safety measures planned based on the risk/benefit evaluation of each product can be appropriately implemented based on the developed PV plan. To develop human resources for appropriate business operat
Job Source: ONO PHARMA USACBRE
Boston, MA, United States
VAS Quality & Risk Management Director Job ID 158433 Posted 26-Apr-2024 Service line Advisory Segment Role type Full-time Areas of Interest Valuations/Appraisal Location(s) Remote - US - Remote - US - United States of America Are you ready to start an exciting career with CBRE? About The Role: As a CBRE Quality & Risk Management (QRM
Job Source: CBREBoston, MA, United States
Takeda Pharmaceuticals Director, PV Risk Management Boston , Massachusetts Apply Now By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Takeda Development Center Americas, Inc. is seeking a Director, PV Risk Management in Cambridge, MA with the following requirements: Master’s degree in Regulatory Affairs, Pharmaceutical Sciences, Public Health, or life sciences or related field or foreign academic equivalent plus 8 years related experience. Prior experience must include: Strategize, author, and review Global and European Risk Management Plans (RMP) Core-RMP, EU-RMP other RMP including those for first or supplementary marketing authorizations applications (NDA submissions); Advise product team on the maintenance and implementation of REMS program for assigned product and support FDA response requests; Support health authority inspections and audits (on behalf of the company) for assigned products including supporting FDA Inspections and MHRA (The Medicines and Healthcare products Regulatory Agency) inspections; Engage in cross-functional strategic discussions for management of activities including planning, authoring and review of periodic aggregate reports like Periodic Benefit-Risk Evaluation Report (PBRER), Development Safety Update Report (DSUR), Periodic Adverse Drug Experience Report (PADER/PAER) in compliance with global regulations. Up to 5% travel required. Up to 100% remote work allowed from anywhere in the US. Apply on-line at www.takedajobs.com and search for Req #R0118571
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
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Email Alert for Director, PV Risk Management jobs in Boston, MA, United States
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