Full-Time

PV Strategy Manager/Senior Manager

Direct Staffing

Direct Staffing

No salary listed

San Francisco, CA, USA

In Person

Category
Business & Strategy (1)
Requirements
  • Bachelor’s degree or equivalent in scientific or quality-related field with significant experience in pharmaceutical industry and/or quality assurance
  • Experience in pharmacovigilance, with demonstrated applied knowledge of pharmacovigilance and international pharmacovigilance regulatory requirements and guidance
  • Experience in compliance program or project management, with demonstrated analytical, organizational and planning skills
  • Proven demonstration of leadership, strategic and system thinking
  • Demonstrated problem solving and decision-making skills
  • Ability to work effectively in an international multicultural matrix organization; highly effective team work and collaboration skills
  • Demonstrated ability to effectively communicate, influence and lead both with and without authority; fluency in written and spoken English
Responsibilities
  • Define and maintain the audit and risk universe of pharmacovigilance processes/activities and perform risk assessment to determine annual audit plan; define and maintain risk assessment methodology and related procedures and tools
  • Assess data/metrics from pharmacovigilance audits, inspections, regulatory intelligence and risk management activities by the business functions for compliance trends and risks; develop communication tools for audits and inspection metrics and trends
  • Define audit scope for internal process and licensing partner audits, review audit plan, audit reports which contain a pharmacovigilance component, and assist evaluation of CAPA as assigned; act as a point of contact for internal process pharmacovigilance and licensing partner audits and support the lead auditor
  • Participate in pharmacovigilance audits, and support regulatory authority pharmacovigilance inspections as necessary
  • Maintain highest level of awareness, expertise in international pharmacovigilance regulations and internal policies and SOPs; assess impact of new regulations and guidance on pharmacovigilance activities
  • Provide quality leadership and direction to PDQ/PDQA and our customers/stakeholders on pharmacovigilance related issues; establish strong partnership with key stakeholders in business functions and represent PDQ/PDQA in cross-functional governance teams
  • Participate in or lead department or cross-functional compliance projects and initiatives as assigned; assist and/or contribute to the development and execution of PDQ/PDQA goals
Desired Qualifications
  • Proficiency in the conduct of pharmacovigilance audits

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