Manager, Pharmacovigilance
Worldwide Clinical Trials
Posted: 10/21/2026
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Posted: 10/21/2026Manager, Pharmacovigilance
Worldwide Clinical TrialsPosted 10/21/2026full-timeRemote • North Carolina • United StatesMid-LevelSenior💰 $90,000 - $178,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in global pharmacovigilance, clinical trial safety processes, and regulatory compliance, while effectively leading and mentoring teams to achieve project goals and maintain high-quality standards.
Highest-signal resume keywords
Global Pharmacovigilance ExperienceClinical Trial Safety ProcessesMentorship and People LeadershipRegulatory Reporting RequirementsStakeholder Management Skills
About the role
Key responsibilities & impact- Lead and oversee pharmacovigilance projects and team operations to ensure compliance with applicable regulations, guidelines, and internal processes
- Manage project delivery against agreed timelines, quality expectations, and budgeted scope of work
- Coach, mentor, and develop team members
- Identify, escalate, and help resolve study, operational, or staff-related issues
- Maintain expertise in global safety regulations, reporting requirements, and pharmacovigilance best practices
- Support project planning, including scope management, proposal reviews, budget discussions, and bid defense participation
- Organize and deliver training initiatives
- Contribute to staff recruitment, onboarding, and professional development
- Represent Pharmacovigilance during sponsor audits
- Contribute to departmental or company-wide initiatives
- Provide leadership support and serve as backup to senior pharmacovigilance leadership
Requirements
What you’ll need- 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
- At least 2 years in a mentorship or people leadership capacity
- Strong knowledge of clinical trial safety processes, pharmacovigilance regulations, regulatory reporting requirements, SOPs, and industry best practices
- Excellent understanding of medical and scientific terminology, adverse event assessment, and safety database technologies
- Proven ability to manage multiple priorities, work independently, and collaborate effectively within matrixed global teams
- Strong interpersonal, presentation, and stakeholder management skills, with experience engaging sponsors, clients, and cross-functional colleagues
- Proficiency in written and verbal English
- Excellent communication, organizational, and attention-to-detail skills
Benefits
Comp & perks- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Professional growth and development opportunities
- Training and professional development initiatives
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Pharmacovigilance RegulationsAdverse Event AssessmentSafety Database TechnologiesSOPsProject ManagementBudget ManagementProposal ReviewsTraining InitiativesRecruitment and OnboardingCompliance Expertise
Soft Skills
Interpersonal SkillsPresentation SkillsAttention to DetailOrganizational SkillsCollaboration Skills
Industry Keywords
Clinical TrialsTherapeutic AreasGlobal Safety RegulationsPharmacovigilance Best PracticesSponsor Audits