Job Description

Home Based - CDMX

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What You Will Be Doing

  • Supporting the collection, review, and processing of adverse event data in accordance with pharmacovigilance regulations and company procedures.
  • Assisting in the preparation and submission of safety reports to regulatory authorities and stakeholders.
  • Collaborating with cross-functional teams to ensure timely and accurate communication of safety information.
  • Contributing to the development and maintenance of pharmacovigilance documentation, including standard operating procedures and safety management plans.
  • Participating in training and development activities to gain a deeper understanding of pharmacovigilance pra...

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