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Associate, Pharmacovigilance

1+ years
Not Disclosed
10 July 18, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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.