Remote Pharmacovigilance Manager

Worldwide Clinical Trials; Charlotte (NC); Remote; USD 90,000 - 178,000; Full time

Job summary

Worldwide Clinical Trials seeks a Manager, Pharmacovigilance to lead PV teams and projects with global reach. This REMOTE US role collaborates across time zones to deliver high-quality safety services for diverse clinical trials.

You will guide teams, ensure regulatory compliance, manage timelines and budgets, and advance patient safety through PV oversight. Strong leadership and cross-functional collaboration are essential.

Qualifications

• Bachelor's degree in a science-related field, nursing, or equivalent experience.
• Minimum 5 years of global pharmacovigilance experience across multiple phases and therapeutic areas.
• Demonstrated leadership with at least 2 years in a mentorship or people leadership capacity.
• Strong knowledge of clinical trial safety processes, regulatory reporting, SOPs, and PV best practices.
• Excellent understanding of medical terminology, adverse event assessment, and PV technologies.
• Proven ability to manage multiple priorities and collaborate within global teams.
• Strong interpersonal, presentation, and stakeholder management skills.

Responsibilities

• Lead and oversee pharmacovigilance projects and team operations to ensure compliance with applicable regulations, guidelines, and internal processes.
• Manage project delivery against agreed timelines, quality expectations, and budgeted scope of work.
• Coach, mentor, and develop team members, providing ongoing guidance and support to promote high performance.
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Skills

Global pharmacovigilance

Leadership

Regulatory reporting

Sponsor/stakeholder mgmt

English proficiency

Education

Bachelor's degree in science or related field

Tools

Safety database systems

Job description

Worldwide Clinical Trials seeks a Manager, Pharmacovigilance to lead PV teams and projects with global reach. This REMOTE US role collaborates across time zones to deliver high-quality safety services for diverse clinical trials.

You will guide teams, ensure regulatory compliance, manage timelines and budgets, and advance patient safety through PV oversight. Strong leadership and cross-functional collaboration are essential.