Pharmacovigilance Associate – Remote (US-Based)
Company: Worldwide Clinical Trials
Location: Durham, NC (Remote - USA)
Job Type: Full-Time | Permanent
Salary: Competitive
Experience Required: Minimum 1 year in Pharmacovigilance
Start Date: 17 July 2025
Closing Date: 16 August 2025
Work Mode: Remote
Job Summary:
Worldwide Clinical Trials, a leading global mid-sized CRO, is seeking a detail-oriented Pharmacovigilance Associate to join its remote US-based team. As part of the dynamic Drug Safety team, you will manage safety data, contribute to safety reporting, and help ensure regulatory compliance during clinical drug development. Ideal for candidates with at least 1 year of pharmacovigilance experience and strong organizational skills.
Key Responsibilities:
Draft and maintain Safety Management Plans for clinical studies
Attend internal/client meetings and present at Investigator Meetings
Review Serious Adverse Event (SAE) data for completeness and accuracy
Enter data into Safety Databases and track incoming safety info
Generate and resolve queries for missing/unclear safety data
Quality check SAEs processed by other associates
Prepare regulatory reports and perform safety submissions
Submit periodic safety updates and reports
Stay current on global pharmacovigilance regulations
Support budget tracking and project scope compliance
May assist in bid defenses, mentoring, or training new PV staff
Required Skills & Qualifications:
Bachelor’s degree in life sciences, nursing, or a related field
Minimum 1 year of experience in pharmacovigilance (clinical trials)
Solid understanding of medical terminology and adverse event assessment
Knowledge of international PV reporting requirements and guidelines
Strong computer skills (Microsoft Office Suite)
Excellent written and verbal communication
Strong organizational skills and attention to detail
Ability to manage competing priorities under tight timelines
Willingness for limited travel (domestic/international) if required
Fluent in English
Perks & Benefits:
100% remote work opportunity
Competitive compensation package
Work with a collaborative and mission-driven global team
Career development and internal mobility
Contribute to the full lifecycle of innovative drug development
Inclusive, diverse work environment
Company Overview:
Worldwide Clinical Trials is a global, mid-sized, full-service CRO with over 3,500 professionals across 60+ countries. We support drug development through creative problem-solving and high-quality research, focusing on delivering life-changing treatments. Our teams are committed to improving lives by advancing clinical research with purpose and innovation.
Work Mode:
Remote (U.S.-based applicants only)
Call to Action:
Looking to advance your pharmacovigilance career in a remote, dynamic, and patient-focused environment? Apply now to join Worldwide Clinical Trials and help bring innovative therapies to life.
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