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10 часов назад

Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence (Pharmacovigilance)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Philippines
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Scientist/Senior Scientist – QPPV Office, Local Safety Support & Regulatory Intelligence (Pharmacovigilance): Providing regional safety oversight for Consumer products across their lifecycle, including new product development, with an accent on safety evaluations, risk management, and cross-functional collaboration. Focus on analyzing complex pharmacovigilance data, identifying clinically relevant safety signals, and translating findings into clinical insights and regulatory safety decisions.

Location: Pasig, Philippines

Company

hirify.global provides safety and regulatory support for Consumer products throughout their lifecycle, including new product development.

What you will do

  • Provide regional safety oversight and contribute to safety deliverables and evaluations across the Consumer product portfolio.
  • Identify, communicate, and manage potential and known safety risks.
  • Partner with the Regional Medical Safety Officer and collaborate with R&D, Regulatory, Quality, and LPV teams.
  • Analyze safety data from post-market reports, literature, and other sources to support safety assessments and reviews.
  • Represent or provide backup to the Regional Medical Safety Officer in meetings and safety deliverables.
  • Communicate clinical safety insights to support product development and post-market safety surveillance strategies.

Requirements

  • Licensed MD with at least 3 years of clinical experience.
  • At least 2 years of industry experience in foundational to intermediate pharmacovigilance.
  • Ability to analyze, interpret, and present complex data in clear scientific language.
  • Understanding of adverse events, serious adverse events, case assessment, safety signals, and benefit-risk considerations.
  • Strong project management, organizational, communication, and presentation skills.
  • Ability to manage multiple products, complex data sets, timelines, and cross-functional activities in an international environment.

Culture & Benefits

  • Collaborative work across multiple functions, lines of business, and regional teams.
  • Exposure to diverse products, safety topics, and complex clinical and regulatory questions.
  • Work according to established SOPs and safety deliverable timelines.
  • Opportunity to contribute assertive, patient- and consumer-focused safety insights.

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