Clinical Research Coordinator

hace 5 días

Madrid Centro, Madrid, España IQVIA A tiempo completo
About the Role

IQVIA is seeking a highly skilled Clinical Research Coordinator / Study Nurse to support a clinical research study at our site in Villamartin. This part-time role is for 24 hours per week and is expected to last approximately 1 year.

Key Responsibilities
  • Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
  • Perform ECG and vital signs.
  • 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.
  • Ensure correct custody of study drug according to site standard operating procedures.
  • Coordinate with the study monitor on study issues and effectively respond to monitor-initiated questions.
  • Order and maintain study supplies.
Requirements
  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting.
  • Experience conducting ECG and taking vital signs.
  • 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 Spanish and English language skills.

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