Position Overview

Our mission is to safeguard patient safety and lead pharmacovigilance (PV) in Japan.

The Senior Manager, Global Patient Safety (GPS) reports to the Director, GPS (Safety Management Officer) in Japan and serves as a core leader for safety operations, overseeing the handling of Individual Case Safety Reports (ICSR), Investigation Reports (RR), and Foreign Measures Taken (FSMT) reports. Additionally, this role proactively drives aggregate reporting, vendor management, and GVP-related activities to ensure both quality and compliance.

What Makes This Role Attractive

Make meaningful impact in a high-stakes safety function as a key member driving Japan’s PV frameworkLead vendors and cross-functional teams to design and implement process improvementsContribute to pivotal documents directly linked to development and post-approval, including J-RMP and J-NDACollaborate globally and gain experience bridging international standards with Japanese regulationsBuild your career through audits and inspections exposure and by managing complex, high-impact projects

Responsibilities

Serve as Japan’s point of contact for ICSR, RR, and FSMT handling, ensuring quality and on-time deliveryLead local aggregate reporting and ensure submissions meet regulatory requirementsMonitor and oversee PV service providers, ensuring performance aligns with contracts and project plansReview provider-prepared assessments and PMDA reports for accuracy and execute improvement actionsDesign and drive continuous process improvements to enhance quality and complianceLead creation and revision of SOPs and plan/execute related training as neededContribute to Japan Risk Management Plan (J-RMP) development and manage planning, execution, and trackingPartner effectively with internal cross-functional teams (Medical Affairs, Regulatory Affairs, Commercial/Marketing, Clinical Development) and license partners to ensure the quality and alignment of PV deliverablesContribute to the safety section of the Japan New Drug Application (J-NDA) and lead resolution of PMDA inquiries

Qualifications

7+ years of hands-on experience in drug safety/pharmacovigilance within the pharma/biotech industryStrong knowledge of PMDA/MHLW/ICH guidelines and regulations governing PV in both clinical trials and post-marketing settingsProven track record of delivering results through cross-functional collaboration with Medical Affairs, Regulatory Affairs, Commercial, and Clinical DevelopmentExperience supporting or leading regulatory authority audits/inspections, including PMDA re-examination, MAH license renewal, and GCP reliability inspectionsProject management experience in complex initiatives such as safety database implementations, function/team improvements, and transfers of business authorizations (including safety data migration)Experience in contracting and managing external service providersPractical experience in global PV

Career Opportunities

Gain a panoramic view of Japan’s safety operations and participate in high-impact decision-makingStrengthen both subject-matter expertise and leadership capabilities through global collaboration and Japanese regulatory engagementBuild a resilient career through deep involvement in key deliverables such as SOPs, J-RMP, and J-NDA

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location.  In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.  For other countries’ specific benefits, please speak to your recruiter.
Please be advised that at Regeneron, we believe we are most successful and work best when we are together.  For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.
 

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.