Clinical Research Associate - IQVIA Biotech
QuintilesIMS
Barcelona, ES
hace 2 días

Responsibilities

  • You will be responsible for ensuring that, at the site level, the Clinical Monitoring Plan is implemented.
  • To ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework.
  • Excellent knowledge of Good Clinical Practice (GCP) and also good working knowledge of conducting clinical trials in general.
  • Experience of performing site start up procedures, routine monitoring and site closure.
  • Excellent interpersonal and organisational skills
  • Ability to manage multiple priorities across various clinical trials
  • Ability to travel.
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