Associate Director, Pharmacovigilance

🔥 0 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $112k - $223k / year

⏰ Full Time

🟠 Senior

👔 Director

🦅 H1B Visa Sponsor

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Lead global pharmacovigilance projects and teams • Ensure activities comply with regulations, quality standards, and project timelines • Provide strategic oversight of staff and project performance • Address risks, issues, and escalations supporting successful study execution • Guide teams on complex safety reporting scenarios and sponsor requirements • Partner with department leadership to enhance processes and implement efficiencies • Support technology and operational improvements • Contribute to proposal development, budget reviews, bid defense meetings, and scope management • Coach, train, recruit, onboard, and develop pharmacovigilance professionals • Represent Pharmacovigilance during sponsor audits, client consultations, and external-facing activities • Participate in business development, conference presentations, marketing, and thought leadership • Contribute to departmental and company-wide initiatives • Provide backup support to senior pharmacovigilance leadership

🎯 Requirements

• Bachelor’s degree in a science-related field, nursing, or equivalent combination of education and relevant experience • Minimum of 8 years of global pharmacovigilance experience supporting pre-approval clinical trials across multiple therapeutic areas and study phases • 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 • 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 • Proficiency in written and verbal English

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Equal employment opportunities • Collaborative and inclusive environment • Growth and development opportunities • Coaching, training, recruitment, onboarding, and professional development opportunities