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Fortrea

Global CRO providing Phase I-IV trials

QPPV Professional

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTaipei City, TaiwanNo salary listedIn-person

About the Job

Requirements

  • Solid pharmacovigilance experience and knowledge of local pharmacovigilance day-to-day operations.
  • Proven experience interacting with sponsors and regulatory authorities.
  • Good English communication and teamwork.

Responsibilities

  • Serve as the main pharmacovigilance contact for the local Health Authority.
  • Set up the local pharmacovigilance system as applicable, including preparing local business operation procedures, and ensure compliance with national pharmacovigilance legislation and global regulatory requirements.
  • Participate in and/or co-host local Health Authority inspections and audits as applicable.
  • Create and implement local pharmacovigilance business continuity activities, including appointing a deputy locally nominated person responsible for pharmacovigilance or backup as applicable.
  • Perform local regulatory intelligence that might affect pharmacovigilance activities, assess the impact of changes, and communicate them timely to the QPPV Office and other relevant stakeholders as applicable.
  • Support translation of documentation to the local language and submissions to local authorities as applicable.
  • Ensure local pharmacovigilance processes follow the EU General Data Protection Regulation and inform the QPPV Office about specific local requirements related to it.
  • If required, act as the locally nominated person responsible for pharmacovigilance toward the local Health Authority and perform relevant activities as per local regulation.
  • Ensure reporting of any individual case safety reports received locally to the global safety mailbox.
  • Assist with follow-up for individual case safety reports in the local language when required.
  • Act as the local subject matter expert for risk management activities.
  • Support preparation of local Risk Management Plans and provide relevant local-specific data for inclusion, as applicable.
  • Ensure local implementation of Risk Management Plans and additional risk minimization measures.
  • Monitor and report on local effectiveness of risk minimization activities.
  • Review and approve locally adapted safety communication materials, including Direct Healthcare Professional Communications.
  • Ensure local literature surveillance, including search strategy, is set up.
  • Ensure local literature surveillance is performed, including reporting relevant safety signals and individual case safety reports from local sources to global safety teams as applicable.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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