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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Director Pharmacovigilance Hub - Americas

Biology & BiotechConfirmed live in the last 24 hours
Full-time$183.1k - $305.2k /yr

About the Job

Requirements

  • A minimum bachelor's degree and 12 or more years of pharmacovigilance experience, with demonstrated achievements in patient safety.
  • Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level.
  • Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner.
  • Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels.

Responsibilities

  • Oversee country- and/or regional-level pharmacovigilance execution within the assigned region, ensuring local safety activities comply with global standards, local regulatory requirements are met, and country-generated safety data are integrated accurately and promptly into the global pharmacovigilance system.
  • Serve as the escalation point for local execution issues and as the conduit between local operations and global oversight functions.
  • Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office leadership informed of updates or changes to local requirements or processes, including standard operating procedure addenda, safety communications, labeling updates, and local submission requirements, in alignment with country-specific regulatory requirements.
  • Track local process status, changes, and risks to drive consistency and continuous improvement for the hub's geographic markets, including maintaining and monitoring a common tool such as a tracker or dashboard.
  • Develop innovative approaches to delivering core activities that integrate new technologies, including artificial intelligence.
  • Ensure country compliance with the global pharmacovigilance quality system, supporting inspections, audits, corrective and preventive actions, and timely resolution of deviations or non-compliance.
  • Serve as the local safety point of contact to coordinate with global Global Patient Safety teams, including PV Enablement, CER, and SS, and non-GPS teams, including Medical Affairs and Regulatory.
  • Guide and inform global teams on local requirements and ensure compliance with local legislation.
  • Coordinate with other pharmacovigilance hubs as needed for contributions to activities and/or local documentation.
  • Shape compliant programs that provide high-quality adverse event reports.
  • Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines.

Desired Qualifications

  • Advanced degree.
  • Experience with artificial intelligence technologies.
  • Experience working within Latin American, U.S., and Canadian markets.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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