Site Research Assistant

7 giorni fa


Milano, Lombardia, Italia IQVIA A tempo pieno
Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Milano

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

  • Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Planning and coordinating logístical 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
  • Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correcting custody of study drug according to site standard operating procedures
  • Coordinating with study monitor on study issues and effectively responding to monitorinitiated questions
  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
  • Good knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Good organizational skills with the ability to pay close attention to detail
  • Italian native speaker with good English language skills


Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Gliwice.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

  • Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Planning and coordinating logístical 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
  • Assisting in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
  • Correcting custody of study drug according to site standard operating procedures
  • Coordinating with study monitor on study issues and effectively responding to monitorinitiated questions
  • BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
  • Good knowledge of clinical trials, combined with indepth knowledge of departmental, protocol and studyspecific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with coworkers, managers and clients
  • Good organizational skills with the ability to pay close attention to detail
  • Polish native speaker with good English language skills
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