Senior CRA for Multi-Sponsor Trials – Italy

Medpace

Varese

In loco

EUR 42.000 - 56.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

Una candidatura apposita per questo posto — un curriculum e una lettera di presentazione personalizzati, perfettamente in linea con l'annuncio.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Flexible work environment
Competitive compensation and benefits
Competitive PTO packages
Structured career paths with growth
Company-sponsored employee events
Employee health and wellness

Descrizione del lavoro

Medpace is seeking an Experienced Clinical Research Associate (CRA) to join the Clinical Monitoring team in Italy. You will conduct site visits, verify investigator qualifications, and ensure protocol and regulatory compliance to support trials from initiation through closeout.

You will manage source data verification, data integrity, and timely reporting while traveling 60-80% nationally. Fluent in English and Italian, you will collaborate with site staff and cross-functional teams to drive

Competenze

  • Master in health-related field.
  • Previous experience as Clinical Research Associate (CRA).
  • Willingness to travel 60-80% nationally.
  • Fluent in English and Italian.

Mansioni

  • Perform site monitoring visits and ensure protocol and regulatory compliance.
  • Verify investigator qualifications, training, facilities, laboratories, equipment, and staff.
  • Perform source data verification and apply good documentation practices (GCP/SOPs).
  • Review regulatory documents and assess site recruitment and retention performance.

Conoscenze

Team collaboration
Communication skills
Presentation skills

Formazione

Master's in health-related field

Strumenti

Microsoft Office

Descrizione del lavoro

Medpace is seeking an Experienced Clinical Research Associate (CRA) to join the Clinical Monitoring team in Italy. You will conduct site visits, verify investigator qualifications, and ensure protocol and regulatory compliance to support trials from initiation through closeout.

You will manage source data verification, data integrity, and timely reporting while traveling 60-80% nationally. Fluent in English and Italian, you will collaborate with site staff and cross-functional teams to drive

Ottieni la revisione del curriculum gratis e riservata.

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