Field-Based Clinical Research Coordinator — Part-Time (Rome)

IQVIA

Roma

In loco

EUR 30.000 - 45.000

Part-time

3 giorni fa
Candidati tra i primi
Generatore di candidature

Fatti notare per questo impiego — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Descrizione del lavoro

IQVIA in Rome, Lazio, seeks a part-time Clinical Research Coordinator for field-based work. The role involves prescreening, data review, and documentation, with a focus on patient screening, consent, and study logistics. You’ll collaborate with monitors and sites to ensure protocol adherence and data integrity.

The ideal candidate has a life sciences degree, strong clinical trials knowledge, and excellent communication. English fluency and solid IT skills are essential for success in this role.

Competenze

  • Bachelor’s degree in life sciences or equivalent.
  • Solid understanding of clinical trials and familiarity with study protocols.
  • Good knowledge of medical terminology.
  • Strong IT skills including MS Office.
  • At least 2 years experience as a Clinical Research Assistant or Coordinator.
  • Excellent interpersonal and communication skills.

Mansioni

  • Prescreening and screening tasks for study enrollment.
  • Review charts from the site database and ensure data quality.
  • Maintain and update study documentation and CRFs.
  • Support patient screening and informed consent processes.
  • Coordinate logistics for study procedures per protocol.
  • Communicate with study monitors and respond to inquiries.
  • Perform general administrative tasks related to the study.

Conoscenze

Clinical research
English fluency
Communication skills
Organizational skills
MS Office
Privacy documentation

Formazione

Bachelor’s degree in life sciences

Strumenti

Outlook
Word
Excel
Access

Descrizione del lavoro

IQVIA in Rome, Lazio, seeks a part-time Clinical Research Coordinator for field-based work. The role involves prescreening, data review, and documentation, with a focus on patient screening, consent, and study logistics. You’ll collaborate with monitors and sites to ensure protocol adherence and data integrity.

The ideal candidate has a life sciences degree, strong clinical trials knowledge, and excellent communication. English fluency and solid IT skills are essential for success in this role.

Ottieni la revisione del curriculum gratis e riservata.
o trascina qui il file.
Similar jobs

Offerte di lavoro simili che vale la pena confrontare

Part-Time Clinical Research Coordinator — Rome
Part-Time Clinical Research Coordinator — Rome

IQVIA Argentina • Roma

In loco
EUR 30.000 - 45.000
Part-Time Clinical Research Coordinator (Rome)
Part-Time Clinical Research Coordinator (Rome)

IQVIA • Roma

In loco
EUR 30.000 - 45.000
Clinical Research Coordinator - part time
Clinical Research Coordinator - part time

IQVIA • Roma

In loco
EUR 30.000 - 45.000
Clinical Research Coordinator - part time
Clinical Research Coordinator - part time

IQVIA Argentina • Roma

In loco
EUR 30.000 - 45.000
Remote Clinical Research Associate - Home Based, Italy
Remote Clinical Research Associate - Home Based, Italy

ScholarshipsAds Inc. • Italia

Remoto
EUR 40.000 - 65.000
Clinical Research Associate, Sponsor Dedicated - Italy
Clinical Research Associate, Sponsor Dedicated - Italy

IQVIA • Milano

In loco
EUR 40.000 - 55.000
Company car
Mobile phone
Attractive benefits package
+2
Site Monitoring Specialist (Italy) – Clinical Research
Site Monitoring Specialist (Italy) – Clinical Research

ScholarshipsAds Inc. • Italia

Remoto
EUR 40.000 - 52.000
Remote Clinical Research Associate (Italy)
Remote Clinical Research Associate (Italy)

worldwide.com • Roma

Ibrido
EUR 42.000 - 56.000
Clinical Research Associate, Site Management - Italy
Clinical Research Associate, Site Management - Italy

IQVIA LLC • Lombardia

In loco
EUR 40.000 - 60.000
Remote CRA II — International Trials (Italy Focus)
Remote CRA II — International Trials (Italy Focus)

Linical Europe • Milano

In loco
EUR 55.000 - 85.000
Home-based flexibility
International clinical trials
Collaborative team environment
+1