AD/Director PV Operations


Princeton
Permanent
USD170000 - USD230000
Clinical Development
PR/533711_1741125891
AD/Director PV Operations

The individual will oversee the daily operations of the Pharmacovigilance function, ensuring adherence to standard operating procedures, policies, industry best practices, and relevant regulations.

Primary Responsibilities:

  • Oversee the daily management and execution of pharmacovigilance (PV) operations.
  • Ensure compliance with regulatory requirements, PV agreements, and internal SOPs.
  • Act as a representative for the Drug Safety and Pharmacovigilance departments on clinical development teams.
  • Supervise the processing of Serious Adverse Events (SAEs) by outsourced vendors and monitor compliance operations.
  • Develop and implement strategies to maintain high-quality standards by analyzing and mitigating compliance risks.
  • Manage SAEs, including case triage, data entry, coding review, and narrative writing.
  • Provide support for safety operations in external submissions, signal detection, and risk management planning.
  • Assist in the preparation of periodic safety reports (e.g., DSUR, PSUR).
  • Ensure the compliant exchange of safety data between the company and its partners.
  • Collaborate with the quality management system in Drug Safety to ensure department standards are met, including training, performance monitoring, continuous improvement actions, and good documentation practices.
  • Work with the QA department to maintain high PV inspection readiness across all regions/countries.
  • Collaborate with contract service providers for case processing, aggregate reporting, and quality management activities.
  • Manage the performance of PV systems.
  • Support root cause analysis of deviations relevant to PV systems.
  • Participate in regulatory inspections and company audits, including FDA/MHRA/EMA PV inspections.
  • Prepare responses to audit findings related to the PV department.
  • Manage reconciliation activities with other departments and vendors.
  • Provide project management support for NDA/MAA submission activities and prepare safety data submissions.
  • Support cross-functional teams in patient narrative efforts.
  • Provide strategic oversight of vendors.
  • Manage the quality and compliance of assignments, including training and mentoring.

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