Part-Time Clinical Research Coordinator – Rome

IQVIA LLC

Roma

In loco

EUR 30.000 - 45.000

Part-time

3 giorni fa
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Descrizione del lavoro

IQVIA in Rome is seeking a Clinical Research Coordinator for a part-time role of 2 hours per week, starting immediately and lasting approximately six months. The position supports a clinical research site with prescreening, data review, and documentation management, including patient consent and privacy records.

The ideal candidate holds a life sciences degree, has trial knowledge, strong IT skills, and at least 2 years in a related clinical role. English fluency is required.

Competenze

  • Bachelor’s degree in life sciences or equivalent education.
  • Solid understanding of clinical trials and study protocols.
  • Excellent knowledge of medical terminology.
  • Strong IT skills including MS Office (Outlook, Word, Excel, Access).
  • At least 2 years as Clinical Research Assistant/Coordinator at a trial site.
  • Fluent in English with strong communication abilities.

Mansioni

  • Prescreening and Screening tasks.
  • Review charts from the site data base.
  • Maintain and update study documentation including CRFs and EDC systems.
  • Support patient screening and enrollment including informed consent.
  • Coordinate study procedures in line with the protocol.
  • Communicate with study monitors and respond to inquiries.
  • Carry out general administrative tasks related to the study.

Conoscenze

MS Office
English fluency
Interpersonal skills
Organizational skills
Clinical research knowledge
Communication

Formazione

Bachelor’s degree in life sciences

Strumenti

Outlook
Word
Excel
Access

Descrizione del lavoro

IQVIA in Rome is seeking a Clinical Research Coordinator for a part-time role of 2 hours per week, starting immediately and lasting approximately six months. The position supports a clinical research site with prescreening, data review, and documentation management, including patient consent and privacy records.

The ideal candidate holds a life sciences degree, has trial knowledge, strong IT skills, and at least 2 years in a related clinical role. English fluency is required.

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