Senior Clinical Research Associate

hace 2 semanas

Madrid, Madrid, España Iqvia A tiempo completo

Job Summary

Iqvia is seeking a highly skilled Senior Clinical Research Associate to join our team as a sponsor-dedicated CRA. As a key member of our global contract research organization, you will work closely with one of our esteemed customers, benefiting from world-class training and mentoring in various therapeutic areas.

Key Responsibilities

  • Perform site selection, initiation, monitoring, and close-out visits to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Support the development of a subject recruitment plan to drive study success.
  • Evaluate site practices for quality and integrity, identifying areas for improvement and implementing corrective actions.
  • Manage progress by monitoring regulatory submissions, recruitment, CRF completion, and data query resolution.
  • Collaborate with study site experts and client representatives to ensure seamless communication and project delivery.

Requirements

  • University degree in a scientific discipline or healthcare.
  • Minimum of 2 years of on-site monitoring experience.
  • Good knowledge of clinical research regulatory requirements.
  • Proficiency in MS Office.
  • Fluency in Spanish and English.
  • Strong organizational, time management, and problem-solving skills.
  • Ability to establish and maintain effective relationships with colleagues, managers, and clients.
  • Willingness to travel.
  • Driver's license class B.

What We Offer

  • Resources for career growth and development.
  • Support for flexible work schedules and work-life balance.
  • Programs to enhance therapeutic knowledge and expertise.
  • An excellent working environment and benefits package.

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