Clinical Research Coordinator

1 giorno fa

Ferrara, Emilia-Romagna, Italia IQVIA A tempo pieno

**Job Summary**

IQVIA is seeking a highly skilled and detail-oriented individual to fill the role of Site Research Assistant. As a pivotal member of our site team, you will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.

**Key Responsibilities**

  • Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
  • Plan and coordinate logistical activity for study procedures according to the study protocol.
  • Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
  • Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
  • Correct custody of study drug according to site standard operating procedures.
  • Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

**Requirements**

  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
  • Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
  • Basic knowledge of medical terminology.
  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.
  • Good organizational skills with the ability to pay close attention to detail.
  • Fluent Italian speaker with good English language skills.

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