Job Description

Worldwide Clinical Trials seeks a Manager of Pharmacovigilance to lead safety operations across global clinical trials. The role combines scientific expertise with team leadership, overseeing project delivery, regulatory compliance, and direct report development while supporting the safe development of new therapies.

Responsibilities

• Lead and oversee pharmacovigilance projects and teams, ensuring regulatory and SOP compliance
• Manage project delivery against quality, timeline, and budget targets; identify and escalate risks
• Coach and mentor direct reports; foster accountability, collaboration, and continuous improvement
• Provide guidance on safety regulations, reporting requirements, and pharmacovigilance best practices
• Represent Pharmacovigilance during sponsor audits; support proposal reviews and SOP development

Requirements

• Bachelor's degree in science, nursing, or equivalent education and relevant experience
• Minimum 5 years of global pharmacovigilance experience in pre-approval clinical trials
• At least 2 years of leadership, mentorship, or supervisory experience
• Strong knowledge of pharmacovigilance regulations, adverse event assessment, and reporting requirements
• Proficiency with safety databases, data extraction, and Microsoft Office applications
• Ability to manage multiple priorities independently and in matrix environments
• Strong interpersonal, presentation, and stakeholder management skills; fluent English

Compensation: $90,000–$178,000 base annually

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