Associate Ii, Pharmacovigilance - Brazil - Remote

Worldwide Clinical Trials

Brasilia, Brazil
**
Serious adverse event (sae) data processing
International regulations and reporting requirements
Management of relational database systems
** Worldwide Clinical Trials is seeking an Associate II in Pharmacovigilance for a remote position in Brasilia, Brazil. The role involves managing Serious Adverse Event data and requires a strong background in pharmacovigilance, along with excellent organizational and communication skills. **

Job Summary

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

Matching Summary

Match Score: 75

** Worldwide Clinical Trials is seeking an Associate II in Pharmacovigilance for a remote position in Brasilia, Brazil. The role involves managing Serious Adverse Event data and requires a strong background in pharmacovigilance, along with excellent organizational and communication skills. **

Skills & Requirements

Must-have

  • Serious Adverse Event (SAE) data processing
  • international regulations and reporting requirements
  • management of relational database systems
  • handle multiple competing priorities

Nice-to-have

  • pioneering, creative approaches
  • collaborative and creative environment
  • passion and purpose

Key Requirements

  • Minimum of 3 years of pharmacovigilance experience
  • Bachelor’s degree in science related field, nursing or equivalent
  • Fluent in written and verbal English

Work Rights

Not specified

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