Global Pharmacovigilance Leader – Remote

Worldwide Clinical Trials; EE. UU.; A distancia; USD 112.000 - 223.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials in the United States is seeking an Associate Director, Pharmacovigilance to lead global safety programs and teams, ensuring patient safety, regulatory compliance, and operational excellence across therapeutic areas.

You will partner with global stakeholders to drive quality, efficiency, and continuous improvement in pharmacovigilance processes and technology while contributing to business growth and client satisfaction.

Formación

• Bachelor’s degree in a science-related field, nursing, or equivalent combination of education and relevant experience.
• 8+ years global pharmacovigilance experience across multiple therapeutic areas and study phases.
• Demonstrated leadership experience, including at least 2 years in a people, project, or departmental leadership capacity.
• Strong knowledge of global pharmacovigilance regulations, safety reporting requirements, adverse event assessment, and clinical trial best practices.
• Proven experience managing budgets, scope, timelines, quality standards, and cross-functional stakeholder relationships.
• Strong understanding of pharmacovigilance systems, relational databases, and Microsoft Office applications, including Excel, PowerPoint, and Word.
• Excellent organizational, interpersonal, presentation, and communication skills with the ability to influence, mentor, and guide teams in a matrix environment.

Responsabilidades

• Lead global pharmacovigilance projects and teams, ensuring activities are delivered in compliance with applicable regulations, quality standards, and project timelines.
• Provide strategic oversight of staff and project performance, addressing risks, issues, and escalations to support successful study execution.
• Guide teams on complex safety reporting scenarios and sponsor requirements, serving as a key point of expertise and decision-making.
• Partner with department leadership to enhance processes, implement efficiencies, and support ongoing technology and operational improvements.
• Contribute to proposal development, budget reviews, bid defense meetings, and scope management activities.
• Support team growth through coaching, training, recruitment, onboarding, and development of pharmacovigilance professionals.
• Represent Pharmacovigilance during sponsor audits, client consultations, and other external-facing activities as needed.
• Participate in business development initiatives, including conference presentations, marketing efforts, and thought leadership activities.
• Act as a key contributor to departmental and company-wide initiatives while providing backup support to senior pharmacovigilance leadership when required.

Conocimientos

PV leadership

Budget management

Stakeholder collaboration

Regulatory knowledge

MS Office

English communication

Educación

Bachelor's degree in science or related field

Herramientas

PV systems

Relational databases

Descripción del empleo

Worldwide Clinical Trials in the United States is seeking an Associate Director, Pharmacovigilance to lead global safety programs and teams, ensuring patient safety, regulatory compliance, and operational excellence across therapeutic areas.

You will partner with global stakeholders to drive quality, efficiency, and continuous improvement in pharmacovigilance processes and technology while contributing to business growth and client satisfaction.