Medical Research Professional

hace 1 semana


Madrid, Madrid, España Iqvia Llc A tiempo completo

About the Role: We are seeking a skilled Clinical Research Coordinator to join our team in Malaga, Spain. This part-time position involves supporting the site with various administrative tasks, ensuring the smooth running of clinical trials, and assisting with patient data collection.

Key Responsibilities:

  • Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction of the Principal Investigator.
  • Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns.
  • 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.
  • Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues.
  • Assist with 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.


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