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Associate Director/Director - Clinical Safety & Pharmacovigilance

Associate Director/Director - Clinical Safety & Pharmacovigilance

soterius, inc.
12-14 Years
Not Disclosed
  • Posted 5 hours ago
  • Be among the first 10 applicants

Job Description

Job Description – Associate Director / Director – Pharmacovigilance

Key Responsibilities

  • Provide strategic and operational leadership for assigned pharmacovigilance projects and teams, ensuring quality, compliance, and timely delivery.
  • Oversee safety operations, including ICSR case processing for clinical trials and post-marketing activities, in accordance with applicable regulations, SOPs, and client requirements.
  • Ensure compliance with global pharmacovigilance regulations, quality standards, contractual commitments, and internal processes.
  • Lead and mentor teams, including resource planning, performance management, training, and capability development.
  • Act as a senior point of contact for internal and external stakeholders and effectively manage client relationships.
  • Drive continuous improvement, process optimization, standardization, and operational efficiency across assigned functions.
  • Provide leadership and representation during client audits, internal audits, and regulatory inspections; oversee responses and CAPA implementation.
  • Monitor quality and operational metrics, identify risks/issues, and ensure timely escalation and resolution.
  • Review and approve relevant SOPs, work instructions, reports, and other functional documentation.
  • Support strategic initiatives, new project implementations, business development activities, and other organizational priorities.

Required Skills & Experience

  • Strong knowledge of pharmacovigilance, drug safety, and global regulatory requirements.
  • Significant experience in pharmacovigilance/safety operations, quality, or a related pharmaceutical/healthcare environment.
  • Proven experience in people leadership, project management, client/stakeholder management, and audit/inspection support.
  • Strong leadership, communication, analytical, decision-making, and problem-solving skills.
  • Ability to work independently, manage multiple priorities, and operate effectively in a global/matrix environment.
  • Experience in process improvement and quality/compliance management.

Educational Requirements

  • Bachelor's/Postgraduate degree or equivalent in Pharmacy, Life Sciences, Medicine, Nursing, Biotechnology, or another relevant scientific/healthcare discipline.
  • Associate Director: Typically, 12+ years of relevant experience.
  • Director: Typically,15+ years of relevant experience, with significant leadership and strategic responsibilities.

More Info

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Key Skills

client stakeholder management

quality compliance

quality compliance management

global regulatory requirements

ICSR case processing

audit inspection support

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