Associate Manager, Global Patient Safety - QPPV Governance

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager to join our Patient Safety QPPV team.

This position resides in the Global Patient Safety (GPS) organization of Regeneron within the QPPV Office functional area, and supports the strategic and operational needs of the EU & UK Qualified Person for Pharmacovigilance (EU QPPV). This position acts as a supporting point of contact for coordinating QPPV Office activities to help the team meet its goals by executing and helping maintain operational plans. In addition, the Associate Manager, QPPV Office Implementation Management will work with Subject Matter Experts within GPS and non-GPS functions, as appropriate. All activities within this role directly support the statutory QPPV function. This position sits within the QPPV Office and reports directly to the EU & UK QPPV.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Work Location: Tarrytown, NY

• Hybrid; 4 days per week on site

• 25% Travel may be required

Discover your role:

• Leadership : Provides tactical support and coordination for QPPV Office activities, including oversight meetings, meetings with subject matter experts, PSMF-related activities, and compliance documentation (e.g., minutes, archiving, document retention). Assists in assessing the needs of the QPPV Office and helps maintain frameworks to ensure that regulatory requirements, internal obligations, and inspection readiness are considered. Helps ensure appropriate structure, procedures, and resources are in place to support the QPPV Office's effectiveness. Recognizes when to raise issues to the EU & UK QPPV or manager for timely resolution.

• Planning and Tracking: Supports achievement of goals for the QPPV Office. Helps organize, maintain, and operate the QPPV oversight framework, including oversight forums and cadence (e.g., QPPV monthly oversight meetings, QPPV Core weekly meetings, quarterly meetings with the LCPPV network, and cross-functional team meetings), in collaboration with the WWOO Director where relevant. Coordinates meeting agendas, decision logs, rationale for escalations, and tracking of open actions. Maintains QPPV delegation records and helps ensure evidence of QPPV authority and influence on the PV system is appropriately documented and archived. Monitors the QPPV mailbox and supports triage of communications to help ensure QPPV awareness and timely action. Helps ensure QPPV meeting outputs are inspection-ready. Supports utilization of appropriate systems within Regeneron to optimize cross-functional communication, planning, and transparency. Adheres to and supports compliance with relevant policies, processes, and procedures. Contributes to process improvements to support consistency, efficiency, and compliance.

• Collaborations : Acts as a liaison in interactions between the QPPV Office and internal partners and, where appropriate, external vendors and collaborators. Supports the EU & UK QPPV's accountability for PSMF accuracy and integrity, including: supporting the PSMF coordinator role during PSMF updates; performing PSMF quality control as needed; supporting tasks related to PSMF process/procedural maintenance, including safety system updates. Supports the QPPV in due diligence activities for acquisitions, mergers, or divestments and helps maintain traceability of QPPV input and decisions. Helps prepare and provide input for internal and external presentations. Helps facilitate decision-making in support of QPPV Office objectives.

• Information : Supports the design and implementation of new processes and tools to help ensure integration across the QPPV Office, GPS, and the broader organization. Manages the QPPV SharePoint site. Helps identify and analyze problems and supports the development of solutions to cross-functional and/or organizational issues. Supports processes for sharing information among QPPV Office stakeholders. Supports QPPV Office business continuity by documenting QPPV coverage arrangements (e.g., handover meetings) and escalation pathways. Helps support QPPV oversight of technology initiatives impacting PV, contributing to proportionate, traceable documentation of technology risk within the QPPV oversight framework.

• Communication: Communicates information and helps coordinate and collaborate across functions by providing information regarding the QPPV Office's needs and services to key stakeholders and GPS leadership. Provides administrative support to the QPPV Office, including preparation of workshops, meeting agendas and minutes, presentations, and summaries of QPPV activities and dashboards. Provides input to support resource prioritization decisions across the QPPV Office's portfolio.

This role requires:

• Masters or Doctoral degree (PhD, PharmD, MD) in a relevant field. Industry/regulatory experience preferred.

• Other post-graduate degree in a related field (e.g., MPH, MSc), generally with 3+ years of relevant experience. Industry/regulatory experience preferred.

• Demonstrated achievements of increasing complexity/responsibility.

• Experience supporting pharmacovigilance and patient safety within a pharmaceutical or biotech environment

• Demonstrable knowledge/exposure to GVP Modules I–XVI, EU pharmacovigilance legislation, and PSMF.

• Excellent written and verbal communication skills; proven ability to work in a matrix organization; established project leadership skills, including problem solving and conflict management.

• Proven track record of interpersonal, influencing, leadership, and project management skills.

• Ability to enable decision making and assess situations in order to minimize risk, make timely and pragmatic decisions, and ability to work through ambiguity.

• Experience/exposure in a QPPV Office, PV Quality, or Compliance function with exposure to EU regulatory inspections preferred.

• Baseline knowledge of US and international regulatory guidances and ability to apply this knowledge to pharmacovigilance activities.

• Maintains high ethical standards, including a commitment to the Company’s values and behaviors.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$98,100.00 - $160,100.00