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Senior PV Associate II

Madrigal Pharmaceuticals
Full-time
Remote friendly (Conshohocken, PA)
United States
$97,000 - $117,000 USD yearly
Operations

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Role Summary

Senior PV Associate II at Madrigal, supporting postmarketing pharmacovigilance activities to maintain patient safety and regulatory compliance. Hybrid role located in Conshohocken, requiring 3 days on-site per week, reporting to the Associate Director, Postmarketing PV.

Responsibilities

  • Assist with oversight of pharmacovigilance vendor activities including assessment, evaluation, tracking and reconciliation of safety information
  • Perform retrospective and in-line quality checks to ensure proper coding and processing of post-marketing reports, including tracking and trending for issues and remediation effectiveness
  • Create and utilize trackers to monitor vendor KPIs
  • Provide review of Individual Case Safety Reports (ICSRs), including case narratives, causality assessments and coding for assigned products
  • Ensure compliance with required timelines for global safety submissions and assist with other PV compliance activities
  • Participate in PV safety team and safety vendor meetings
  • Distribute and track meeting minutes with vendors and monthly reports
  • Provide safety information when requested by management
  • Ensure adherence to global regulations, SOPs, and best practices in postmarketing safety
  • Assist with inspection readiness and support audits or health authority inspections as needed
  • Other duties as assigned

Qualifications

  • Bachelorβ€šΓ„Γ΄s degree in relevant scientific discipline. Clinical experience (e.g., RN, BSN, or PharmD) is preferred but not required
  • Minimum of 3 years of relevant experience in postmarketing pharmacovigilance
  • Experience with ICSR processing, narrative writing and quality review
  • Working knowledge of global pharmacovigilance regulations (ICH E2A/B, FDA, EMA)
  • Familiarity with safety databases (Argus, ARISg), MedDRA and WHO Drug coding
  • Strong understanding of safety and pharmacovigilance principles
  • Excellent attention to detail and commitment to high-quality deliverables
  • Collaborative mindset with strong cross-functional communication skills
  • Comfortable operating in a fast-paced, evolving biotech environment
  • Proactive approach to identifying potential safety issues and recommending solutions
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