Remote Global Pharmacovigilance Manager

Worldwide Clinical Trials; United States; Remote; USD 90,000 - 178,000; Full time

Job summary

Worldwide Clinical Trials in the United States is seeking an experienced Manager of Pharmacovigilance to lead high-quality safety activities across global trials. You will guide teams, oversee project delivery, and ensure compliance with international reporting standards.

This leadership role emphasizes mentoring, cross-functional collaboration, and optimizing processes to advance patient safety. You will work remotely from the US and engage with sponsors and global teams.

Qualifications

• Bachelor's degree in a science-related field or equivalent experience.
• Minimum 5 years of global pharmacovigilance with pre-approval trials.
• At least 2 years in people leadership or mentorship.
• Strong knowledge of clinical trial safety processes and regulations.
• Experience with adverse event assessment and safety databases.

Responsibilities

• Lead pharmacovigilance projects, ensuring regulatory compliance.
• Manage delivery against timelines, quality, and scope.
• Coach and develop team members to promote high performance.
• Identify issues and support successful study outcomes.
• Maintain expertise in global safety regulations and reporting.
• Support planning activities including scope, budget, and bids.
• Organize training, recruitment, and professional development.
• Represent Pharmacovigilance during sponsor audits.
• Provide leadership support to senior PV leadership as needed.

Skills

Leadership

Pharmacovigilance

Regulatory knowledge

Stakeholder management

Project management

Communication

English proficiency

Education

Bachelor's degree

Job description

Worldwide Clinical Trials in the United States is seeking an experienced Manager of Pharmacovigilance to lead high-quality safety activities across global trials. You will guide teams, oversee project delivery, and ensure compliance with international reporting standards.

This leadership role emphasizes mentoring, cross-functional collaboration, and optimizing processes to advance patient safety. You will work remotely from the US and engage with sponsors and global teams.