Remote Associate Director, Pharmacovigilance

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 112,000 - 223,000; Full time

Job summary

Worldwide Clinical Trials is seeking an Associate Director, Pharmacovigilance to lead global PV programs across therapeutic areas. You will ensure patient safety, regulatory compliance, and quality while directing teams across time zones.

This REMOTE role is open to US candidates, offering opportunities to drive process improvements, support audits, and contribute to business development while mentoring staff. The company emphasizes collaboration, growth, and impact in clinical research.

Qualifications

• Bachelor’s degree in a science-related field, nursing, or equivalent experience.
• Minimum of 8 years of global pharmacovigilance experience.
• Demonstrated leadership experience (2+ years in leadership role).
• Strong knowledge of global pharmacovigilance regulations and safety reporting.
• Experience managing budgets, scope, timelines, and cross-functional stakeholders.

Responsibilities

• Lead global pharmacovigilance projects in compliance with regulations and timelines.
• Provide strategic oversight of staff and project performance.
• Guide teams on complex safety reporting and sponsor requirements.
• Partner with leadership to improve processes and implement efficiencies.
• Contribute to proposals, budget reviews, and scope management.
• Mentor pharmacovigilance professionals and support audits.

Skills

Global pharmacovigilance

Leadership

Budget management

Stakeholder management

Regulatory knowledge

Pharmacovigilance systems

Microsoft Office

English proficiency

Education

Bachelor’s degree in science-related field or nursing

Tools

Relational databases

Clinical trial systems

Job description

Worldwide Clinical Trials is seeking an Associate Director, Pharmacovigilance to lead global PV programs across therapeutic areas. You will ensure patient safety, regulatory compliance, and quality while directing teams across time zones.

This REMOTE role is open to US candidates, offering opportunities to drive process improvements, support audits, and contribute to business development while mentoring staff. The company emphasizes collaboration, growth, and impact in clinical research.