Clinical Data Reviewer

hace 4 días


Buenos Aires, Buenos Aires C.F., Argentina IQVIA Argentina A tiempo completo
Role Summary
We are looking for a highly motivated and organized Pharmacovigilance Specialist to join our team at IQVIA Argentina. As a critical member of our team, you will be responsible for managing safety data and information, working closely with senior team members to ensure compliance with regulatory requirements.

Key Responsibilities:
  • Managing safety data according to regulatory requirements and project specifications.
  • Performing pharmacovigilance activities, including data collection, tracking, and analysis.
  • Collaborating with cross-functional teams and external partners to achieve project goals.
  • Mentoring junior colleagues and contributing to departmental initiatives.

Requirements:

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

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