Manager, Pharmacovigilance (US)

Lifelancer Ltd; EUA; Teletrabalho; USD 90 000 - 178 000; Tempo integral

Resumo da oferta

Worldwide Clinical Trials in the United States is seeking a Manager, Pharmacovigilance (US) to lead PV activities across multiple trials in a remote US setting (NC). The role combines scientific oversight with people leadership to ensure safety and regulatory compliance.

You'll mentor PV professionals, manage delivery against timelines and budgets, and collaborate across functions to support ongoing study execution and continuous process improvement.

Qualificações

• Bachelor's degree in a science-related field, nursing, or equivalent experience.
• Minimum 5 years of global pharmacovigilance experience across multiple phases/therapeutic areas.
• Leadership experience of at least 2 years in mentorship or supervision.

Responsabilidades

• Lead PV projects and teams in compliance with regulations and SOPs.
• Manage delivery against quality, timelines, and budgets.
• Coach and develop direct reports, fostering accountability.
• Advise on safety regulations, reporting, and best practices.

Conhecimentos

Leadership

Mentorship/People development

Stakeholder management

Interpersonal skills

Presentation skills

Cross-functional collaboration

Time management

Formação académica

Bachelor's degree in a science-related field

Nursing

Equivalent combination of education and relevant experience

Ferramentas

Microsoft Office

Safety databases

Descrição da oferta de emprego

Position Summary

Job Title: Manager, Pharmacovigilance (US). Job Location: Virtual United States North Carolina. Job Location Type: Remote. Job Contract Type: Full-time. Job Seniority Level: Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Manager, Pharmacovigilance at Worldwide Lead the delivery of high-quality pharmacovigilance activities that support the safe development of new therapies across a variety of clinical trial phases and therapeutic areas. In this role, you'll combine scientific expertise, operational oversight, and people leadership to help ensure patient safety and regulatory compliance across global studies. You'll guide and develop pharmacovigilance professionals while overseeing project delivery, quality, timelines, and scope. Your ability to mentor teams, collaborate across functions, and navigate complex safety requirements will directly contribute to successful study outcomes. This is an opportunity to make a meaningful impact by driving excellence in pharmacovigilance operations, supporting continuous improvement initiatives, and serving as a trusted partner to both internal teams and external stakeholders.

Responsibilities

• Lead and oversee pharmacovigilance projects and teams, ensuring activities are conducted in compliance with applicable regulations, SOPs, and project requirements.
• Manage project delivery against quality, timeline, and budget expectations while proactively identifying and escalating risks or issues.
• Coach, mentor, and develop direct reports, fostering a culture of accountability, collaboration, and continuous improvement.
• Provide guidance on safety-related regulations, reporting requirements, and pharmacovigilance best practices across assigned projects.
• Monitor project scope and resource requirements, escalating potential changes and supporting operational efficiency.
• Support departmental activities such as recruitment, onboarding, training, and knowledge-sharing initiatives.
• Contribute to proposal reviews, budget discussions, bid defense meetings, and SOP development as needed.
• Represent Pharmacovigilance during sponsor audits and act as a backup to senior PV leadership when required.
• Participate in departmental and company-wide initiatives that enhance operational excellence and service delivery.

Qualifications

• Bachelor's degree in a science-related field, nursing, or an equivalent combination of education and relevant experience.
• Minimum 5 years of global pharmacovigilance experience supporting pre-approval clinical trials across multiple phases and therapeutic areas.
• Demonstrated leadership experience, including at least 2 years in a mentorship, supervisory, or people-development capacity.
• Strong knowledge of pharmacovigilance regulations, adverse event assessment, regulatory reporting requirements, SOPs, and accepted clinical trial practices.
• Experience working with safety databases, data extraction processes and Microsoft Office applications, including Excel, Word, and PowerPoint.
• Proven ability to manage multiple priorities, work independently, and collaborate effectively within a matrix environment.
• Strong interpersonal, presentation, and stakeholder management skills with experience interacting confidently with sponsors, clients, and cross-functional teams.
• Fluency in written and verbal English.

Additional Information

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is: United States of America - $90,000.00 - $178,000.00