Clinical Trial Associate

hace 5 días


Buenos Aires, Buenos Aires C.F., Argentina IQVIA Argentina A tiempo completo

Career Opportunity

This is an exceptional chance to work as a Clinical Trial Associate in our pharmacovigilance team at IQVIA Argentina. You will be responsible for reviewing, analyzing, and processing safety data from various sources, ensuring compliance with applicable regulations and guidelines.

Main Responsibilities

  1. Analyze and process safety data according to regulatory standards, SOPs, and project demands.
  2. Collect and track AEs and endpoint information, identify initial/update status, input data into databases, categorize AEs and products, compose narratives, and execute literature-related tasks.
  3. Verify that quality, productivity, and delivery benchmarks are achieved per project specifications.
  4. Interact with multifunctional teams and medical professionals to address project-related challenges.
  5. Coach junior team members and assist in departmental projects as delegated by the supervisor.

Requirements

  1. Bachelor's degree in life sciences or a related field.
  2. Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience.
  3. Fluency in English, Spanish, and French.


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