Associate Director, Pharmacovigilance (US) Job at Worldwide Clinical Trials, Durham, NC

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  • Worldwide Clinical Trials
  • Durham, NC

Job Description

Associate Director of Pharmacovigilance at a global CRO, leading pharmacovigilance projects and teams across clinical development programs. This remote role requires strategic oversight of safety reporting, regulatory compliance, and team management to support clinical research delivery.

Responsibilities

  • Lead global pharmacovigilance projects and teams ensuring regulatory compliance and quality standards
  • Provide strategic oversight of staff performance, addressing risks and escalations
  • Guide teams on complex safety reporting scenarios and sponsor requirements
  • Partner with leadership to enhance processes and implement operational improvements
  • Support team development through coaching, training, and recruitment of pharmacovigilance professionals

Requirements

  • Bachelor's degree in science-related field or nursing
  • Minimum 8 years global pharmacovigilance experience in pre-approval clinical trials
  • At least 2 years demonstrated leadership experience managing people or projects
  • Strong knowledge of global pharmacovigilance regulations and safety reporting requirements
  • Experience managing budgets, timelines, and cross-functional stakeholder relationships
  • Proficiency with pharmacovigilance systems, databases, and Microsoft Office applications
  • Excellent written and verbal English communication skills

Compensation: $112,000–$223,000 base

Job Tags

Work at office, Remote work

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