Safety Officer (Pharmacovigilance)

Pasig , Philippines

AI overview

Oversee regulatory monitoring and reporting processes while collaborating with teams to enhance pharmacovigilance practices and ensure compliance with local health authority requirements.

Responsibilities:

Safety Management & Reporting

  • Perform regulatory monitoring for impact on vigilance activities and responsibilities.
  • Perform reconciliation with other departments (distributors, third parties, vendors, and internal stakeholders).
  • Maintain oversight of proper identification of local literature articles for AE reporting as required.
  • Perform reporting/ submissions of safety reports/ updates/information (e.g., SAE, SUE, SUSARs, PSUR, RMP) to local health authorities and departments as applicable.
  • Receive and support the Area Safety lead in the responses to safety-related health authority queries in the territory.
  • Supporting Area Safety Lead in notifying local health authorities of any safety issues including SSI/ESI and Signals.
  • Maintain up-to-date knowledge of local requirements for pharmacovigilance, cosmetic and device vigilances including reporting requirements (for all applicable product classes in the territory) and collaborating with the global team to implement process changes required for identification of new requirements.
  • Record self-identified non-conformances and collaborating with the global team to investigate non-conformances while developing and implementing effective CAPAs.
  • Perform other agreed tasks assigned by manager.
  • Perform document management and archiving as required.
  • Perform training on safety reporting responsibilities of LOC personnel and maintenance of awareness of safety reporting in general.
  • Perform translation for ICSR and PV-related documents, as required

Requirements:

  • Health care science professional e.g.: (nurse, pharmacist, life science degree) or equivalent training and experience.
  • 1-2 years of relevant experience.
  • Pharmaceutical industry experience including product vigilance responsibility role.
  • Sound knowledge of general medicine, pharmacy, and clinical practice, or another relevant scientific/medical field.  
  • Sound knowledge of medical terminology  
  • Computer literate.
  • Good verbal and written communication skills.
  • Ability to establish and maintain open relationships within the organization and with authorities.
  • Fluency in the national language(s) and the English language.

 

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and make a meaningful impact on global healthcare!  

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