Part-Time Clinical Research Coordinator (Rome)

IQVIA

Rodano

On-site

EUR 30,000 - 45,000

Part time

2 days ago
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Job summary

IQVIA is recruiting a part-time Clinical Research Coordinator to support a clinical site in Milano. The role is 20 hours per week with immediate start and a 6-month duration, performing administrative and clinical tasks to ensure smooth trial execution.

The candidate will maintain study documentation, assist with screening and enrollment, and coordinate with monitors and lab operations while using IRT/IWRS and EDC systems. English fluency is required.

Qualifications

  • Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting.
  • 2+ years clinical trial site experience required.
  • Experience with prescreening, screening, CRFs, EDC, eTMF.
  • Experience with IRT/IWRS systems.
  • Fluency in English.

Responsibilities

  • Prescreening and screening tasks.
  • Review charts from the site database.
  • Maintain and update study documentation (protocols, CRFs, EDC, eTMFs).
  • Support patient screening and enrollment, including informed consent.
  • IP-site accountability including IP-patient compliance.
  • Use of IRT/IWRS for randomization and trial operations.
  • Process and ship lab samples.
  • Patient scheduling support.
  • Print and certify EMR.
  • Coordinate study procedures per protocol.
  • Communicate with study monitors and respond to inquiries.
  • Carry out general administrative tasks.

Skills

Interpersonal skills
Communication skills
Organizational skills
Medical terminology
MS Office
English fluency

Education

Bachelor’s degree in life sciences

Tools

IRT/IWRS systems
EDC systems

Job description

IQVIA is recruiting a part-time Clinical Research Coordinator to support a clinical site in Milano. The role is 20 hours per week with immediate start and a 6-month duration, performing administrative and clinical tasks to ensure smooth trial execution.

The candidate will maintain study documentation, assist with screening and enrollment, and coordinate with monitors and lab operations while using IRT/IWRS and EDC systems. English fluency is required.

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