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Clinical Research Coordinator

hace 2 meses


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

We are seeking a highly organized and detail-oriented Site Research Assistant to join our team at IQVIA. As a pivotal member of our site team, you will be responsible for supporting the site in conducting clinical trials in the field of Cardiology.

Key Responsibilities
  • Study Management: Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
  • Logistical Coordination: Plan and coordinate logistical activity for study procedures according to the study protocol.
  • Data Management: Enter data, check data quality, and resolve queries to ensure adherence to study protocol and quality control for content accuracy and completeness.
  • Study Enrollment: Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
  • Study Drug Management: Correctly manage study drug according to site standard operating procedures.
  • Monitor Coordination: Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
Requirements
  • Education: BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
  • Clinical Trials Knowledge: Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.
  • Medical Terminology: Basic knowledge of medical terminology.
  • IT Competence: Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
  • Interpersonal Skills: Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients.
  • Organizational Skills: Good organizational skills with the ability to pay close attention to detail.