Senior Associate, Pharmacovigilance - Mexico/brazil - Remote

Worldwide Clinical Trials

Mexico
Fully remote
Serious adverse event (sae) data processing
Safety management plan authoring
Regulatory reporting and submissions
Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for remote positions in Mexico and Brazil. The ideal candidate will have at least five years of experience in pharmacovigilance and a strong understanding of clinical trial regulations, contributing to the company's mission to improve patient lives through innovative solutions

Job Summary

  • Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements.
  • Independently serves as Lead PV Associate on large sized studies/programs that are moderate to complex in scope of work.
  • We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.

Matching Summary

Match Score: 85

Worldwide Clinical Trials is seeking a Senior Associate in Pharmacovigilance for remote positions in Mexico and Brazil. The ideal candidate will have at least five years of experience in pharmacovigilance and a strong understanding of clinical trial regulations, contributing to the company's mission to improve patient lives through innovative solutions.

Skills & Requirements

Must-have

  • Serious Adverse Event (SAE) data processing
  • Safety Management Plan authoring
  • Regulatory reporting and submissions
  • Medical and scientific terminology
  • International regulations and reporting requirements

Nice-to-have

  • Positive attitude and professional interaction
  • Adaptability and flexibility in tasks
  • Creative and innovative approaches

Key Requirements

  • Bachelor’s degree in a science-related field, or nursing, or equivalent
  • Minimum of 5 years of pharmacovigilance experience
  • Fluent in written and verbal English

Work Rights

Not specified

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