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Regulatory Compliance Officer

1 tydzień temu

Warszawa, Mazovia, Polska IQVIA LLC Pełny etat

Clinical Research Associate - IQVIA Biotech Poland

IQVIA Biotech is hiring a Clinical Research Associate to manage clinical trial sites.

Join IQVIA and play a critical role in the success of our clinical trials.

Job Description
The Clinical Research Associate will be responsible for performing monitoring and site management tasks to ensure compliance with study protocols, regulations, and sponsor requirements.

Key Accountabilities

  • Selecting and managing clinical trial sites, with a focus on maintaining high-quality documentation.
  • Developing and implementing subject recruitment strategies in collaboration with the development team.
  • Maintaining effective communication with assigned sites and delivering protocol and study-related training.
  • Ensuring the quality and integrity of site practices and addressing any quality issues promptly.
  • Tracking and resolving issues related to regulatory submissions, recruitment, case report forms, and data queries.

Requirements

  • A degree in a healthcare or scientific field or equivalent education.
  • At least 2 years of experience in on-site clinical trial monitoring, preferably in CVRM/Oncology.
  • Strong written and verbal communication skills, including proficiency in Polish and English languages.