Associate Director, Pharmacovigilance
Worldwide Clinical Trials
Posted: 10/21/2026
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Posted: 10/21/2026Associate Director, Pharmacovigilance
Worldwide Clinical TrialsPosted 10/21/2026full-timeRemote • North Carolina • United StatesSenior💰 $112,000 - $223,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in global pharmacovigilance, including leadership in clinical trials and compliance with safety reporting regulations. Proven ability to enhance processes, manage budgets, and develop pharmacovigilance professionals while ensuring project timelines and quality standards are met.
Highest-signal resume keywords
Global Pharmacovigilance ExperienceLeadership in Project ManagementKnowledge of Safety Reporting RegulationsBudget Management SkillsProficiency in Microsoft Office Applications
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- 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
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
PharmacovigilanceAdverse Event AssessmentClinical Trial Best PracticesProject Performance OversightRisk ManagementProposal DevelopmentScope ManagementSafety ReportingCross-Functional Stakeholder ManagementOperational Improvements
Soft Skills
Organizational SkillsInterpersonal SkillsPresentation SkillsCommunication SkillsCoaching and Training
Tools & Technologies
Pharmacovigilance SystemsRelational DatabasesMicrosoft ExcelMicrosoft PowerPointMicrosoft Word
Industry Keywords
PharmacovigilanceClinical TrialsRegulatory ComplianceQuality StandardsTherapeutic Areas