Clinical Research Associate

3 tygodni temu

Warszawa, Mazovia, Polska IQVIA Pełny etat

IQVIA is seeking a Clinical Research Associate

As a Clinical Research Associate at IQVIA, you will play a critical role in ensuring the success of our clinical trials. Your primary responsibility will be to perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Key Responsibilities:

  • Perform site selection, initiation, monitoring, and close-out visits, plus maintain appropriate documentation
  • Support the development of a subject recruitment plan
  • Establish regular lines of communication and administer protocol and related study training to assigned sites
  • Evaluate the quality and integrity of site practices – escalate quality issues as appropriate
  • Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Requirements:

  • A Bachelor's degree in a healthcare or other scientific discipline or educational equivalent
  • Experience in on-site monitoring of clinical trials
  • Alternatively, you should have an equivalent combination of education, training, and experience
  • Written and verbal communication skills, including good command of Polish and English language

About IQVIA:

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://www.iqvia.com/

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