Principal, Pharmacovigilance / Device Vigilance

POSITION SUMMARY

The Principal, Pharmacovigilance / Device Vigilance is a detail-oriented and proactive professional supporting the safety surveillance of In Vitro Diagnostic and Software-driven products across their lifecycle, including clinical studies and post-market activities. This role is responsible for the collection, assessment, reporting, and management of adverse events, product complaints, and safety data for both medicinal products and medical devices, ensuring compliance with global regulatory requirements.

The position plays a critical role in ensuring compliance with global regulatory requirements (e.g., FDA, EU IVDR, Japan) and maintaining the highest standards of patient safety and product quality across both laboratory-developed tests and regulated IVD products, including software/algorithm-based components.

PRIMARY RESPONSIBILITIES

• Pharmacovigilance (Drug Safety)
  • Perform case intake, triage, and processing of Individual Case Safety Reports (ICSRs)
  • Process and evaluate adverse events associated with diagnostic use (e.g., clinical impact of false positives/negatives)
  • Coordinate medical review and causality assessment of adverse events
  • Coordinate timely submission of safety reports (e.g., MedWatch, EudraVigilance, CIOMS)
  • Support aggregate reporting (PSUR/PBRER, DSUR, annual reports)
  • Maintain and ensure compliance with global PV regulations (FDA, EMA, ICH, etc.)
  • Contribute to signal detection and risk management activities
• IVD Device Vigilance
  • Review, triage, and assess product complaints and adverse events related to genetic and diagnostic testing, including incorrect, delayed, or misinterpreted results
  • Evaluate reportability of events under FDA (MDR), EU IVDR vigilance, Japan and other global regulations
  • Prepare and submit Medical Device Reports (MDRs) and vigilance reports within regulatory timelines
  • Collaborate with laboratory operations, bioinformatics, and software teams to investigate root cause (e.g., assay performance, variant interpretation, software defects)
  • Support post-market surveillance activities, including trending, signal detection, and periodic safety reporting
• Software & Algorithm-Related Safety
  • Assess safety events associated with software as part of a medical device system, including algorithm errors, data processing issues, and reporting inaccuracies
  • Partner with engineering and data science teams to evaluate software-related complaints and implement corrective actions