Clinical Research Associate

hace 2 semanas


Madrid, Madrid, España IQVIA A tiempo completo
About the Role

Clinical Research Associates are vital to the success of our Sponsor dedicated team at IQVIA. As a junior CRA, you will be responsible for performing site selection, initiation, monitoring, and close-out visits.

Your Responsibilities:
  • Conduct thorough site assessments to ensure compliance with regulatory requirements
  • Support the development of subject recruitment plans to optimize study outcomes
  • Evaluate the quality and integrity of site practices, adhering to Good Clinical Practice and International Conference on Harmonization guidelines
  • Manage progress by tracking regulatory submissions, case report form completion, and data query resolutions
  • Collaborate with experts at study sites and client representatives to achieve study objectives
Requirements

To succeed in this role, you will need:

  • A university degree in a scientific discipline or healthcare
  • Experience in the Pharma Industry or Clinical Trials environment
  • Excellent computer skills, including MS Office
  • Proficiency in Spanish and English language
  • Strong organizational, time management, and problem-solving skills
  • The ability to establish and maintain effective working relationships
  • Flexibility to travel and hold a valid driver's license class B
What We Offer

We provide:

  • A comprehensive benefits package, including company car and mobile phone
  • A stable, international work environment with opportunities for career growth
  • A flexible work schedule and supportive leaders
  • Resources to build your therapeutic knowledge and expertise
About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We strive to create a healthier world by pushing the boundaries of human science and data science.



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