Adverse Event Review Specialist

hace 3 semanas


San José, San José, Costa Rica Pfizer A tiempo completo
Job Summary

We are seeking an experienced Adverse Event Review Specialist to join our team at Pfizer. As a key member of our pharmacovigilance department, you will play a crucial role in ensuring the safety profile of our products and meeting regulatory requirements.

Key Responsibilities:
  • Report Review and Processing: You will be responsible for reviewing and processing reports of adverse drug experiences, identifying and prioritizing cases, assessing complexities, and documenting case narratives.
  • Regulatory Compliance: Your tasks will include generating reports that adhere to regulatory compliance timelines, liaising with stakeholders, including Pfizer Country Organizations and Clinical Development, and developing expertise on Pfizer's products and regulations.
Requirements:
  • Bachelor's Degree: A Bachelor's degree in a science-related field, pharmacy, or nursing is required. Healthcare professional qualification is preferred.
  • Communication Skills: Excellent communication and computer literacy skills are essential for this role.
  • Language Fluency: Fluency in spoken and written English is mandatory.
Estimated Salary:

$70,000 - $100,000 per year, depending on experience.

Work Location:

This position is located on premise.

About Pfizer:

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.



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