Clinical Research Coordinator

2 settimane fa

Ferrara, Emilia-Romagna, Italia IQVIA A tempo pieno

Are you looking for an opportunity or a new challenge in Clinical Research? Do you want to work for an industry leading company? IQVIA is currently recruiting for a
Clinical Research Coordinator to support a site in Cona Ferrara.


This part time role (15h per week)
with an immediate start for about 6 months is to support the site in
Cona Ferrara in conducting a clinical trial.


The preferred working hours are:
Monday, Tuesday and Wednesday: 9:00-13:00, Thursday: 9:00-12:00.


As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.


Day to day responsibilities will include:

  • Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
  • Maintain uptodate study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
  • Plan and coordinate logístical activity for study procedures according to the study protocol
  • 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
  • Correct custody of study drug according to site standard operating procedures
  • Coordinate with study monitor on study issues and effectively respond 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, nurse, medical assistant, other medical profession
  • Basic 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 client
  • Good organizational skills with the ability to pay close attention to detail.
  • Italian native speaker and good English language skills

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