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Clinical Research Coordinator

2 mesi fa

Ferrara, Emilia-Romagna, Italia IQVIA Argentina A tempo pieno
Job Opportunity at IQVIA Argentina

We are seeking a highly skilled and detail-oriented individual to join our team as a Site Research Assistant. This role will provide support to a clinical research study and ensure the smooth running of the clinical trial.

Key Responsibilities:
  • Maintain up-to-date study protocols, case report forms, and Electronic Data Capture systems
  • Plan and coordinate logistical activities for study procedures
  • Enter and quality-check data to ensure adherence to study protocol and quality control
  • Assist in study enrollment by recruiting, screening, and orienting volunteers
  • Coordinate with study monitor on study issues and respond to monitor-initiated questions
Requirements:
  • BS/BA in life sciences or equivalent and/or relevant work experience in a clinical environment
  • Good knowledge of clinical trials and departmental operating procedures
  • Basic knowledge of medical terminology
  • Strong IT competence and excellent interpersonal skills
  • Good organizational skills and attention to detail
  • Fluent Italian speaker with good English language skills

If you are a motivated and organized individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.