Pharmacovigilance Specialist

hace 6 días


Ciudad de México, Ciudad de México IQVIA A tiempo completo

Job Overview

As a Pharmacovigilance Specialist at IQVIA, you will play a critical role in ensuring the safety and efficacy of pharmaceutical products in clinical trials. Under moderate supervision, you will execute feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.

Key Responsibilities

  • Execute pharmacovigilance processes applicable to Research Sites and Units (RSU).
  • Submit safety reports (periodic and expedited) in a timely manner.
  • Submit Serious Adverse Events (SAE) and Suspected Unexpected Serious Adverse Reactions (SUSAR) to the Regulatory Authority (RA) on time, in accordance with regulatory timelines.
  • Perform tasks at a country level associated with Site Activation (SA) activities, in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines.
  • May also include maintenance activities, such as ensuring compliance with regulatory requirements and updating relevant documentation.

Requirements

To be successful in this role, you will need:

  • A Bachelor's Degree in Life Sciences or a related field.
  • 1-2 years of experience in pharmacovigilance, preferably in clinical studies.
  • Fluency in conversational English.

At IQVIA, we are committed to pushing the boundaries of human science and data science to make a meaningful impact on the life sciences industry. If you are passionate about ensuring the safety and efficacy of pharmaceutical products, we encourage you to apply for this exciting opportunity.



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