Remote Pharmacovigilance Manager – Global Trials

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 90,000 - 178,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Manager, Pharmacovigilance to lead global pharmacovigilance projects, ensuring patient safety and regulatory compliance across multiple trials.

You will mentor PV professionals, manage timelines and budgets, and drive continuous process improvements in a collaborative, matrixed environment.

This remote US-based role offers exposure to diverse therapeutic areas, sponsor interactions, audits, and opportunities to shape PV strategy and team development.

Qualifications

• Bachelor's degree in a science-related field or nursing.
• Minimum 5 years of global pharmacovigilance experience across trials.
• 2+ years in mentorship or people leadership.
• Strong knowledge of pharmacovigilance regulations and regulatory reporting.
• Experience with adverse event assessment and safety databases.
• Ability to manage multiple priorities in a global matrix.
• Excellent communication and stakeholder management in English.

Responsibilities

• Lead PV projects and ensure regulatory compliance across trials.
• Manage delivery against timelines, quality, and budgeted scope.
• Coach and develop team members for high performance.
• Identify and resolve study or staff-related issues to support outcomes.
• Maintain expertise in global safety regulations and reporting.
• Support planning activities, including budgets and bids.

Skills

Leadership

Mentorship

Stakeholder management

Communication

Team leadership

English proficiency

Education

Bachelor's degree in science-related field or nursing

Tools

Safety database technologies

Job description

Worldwide Clinical Trials is seeking a Manager, Pharmacovigilance to lead global pharmacovigilance projects, ensuring patient safety and regulatory compliance across multiple trials.

You will mentor PV professionals, manage timelines and budgets, and drive continuous process improvements in a collaborative, matrixed environment.

This remote US-based role offers exposure to diverse therapeutic areas, sponsor interactions, audits, and opportunities to shape PV strategy and team development.