Job Search and Career Advice Platform

Attiva gli avvisi di lavoro via e-mail!

Lead Clinical Research Associate – Italy

Resourcing Life Science

Italia

In loco

EUR 30.000 - 50.000

Tempo pieno

Oggi
Candidati tra i primi

Genera un CV personalizzato in pochi minuti

Ottieni un colloquio e una retribuzione più elevata. Scopri di più

Descrizione del lavoro

A global CRO organization is seeking a Clinical Research Associate (CRA) in Italy. The role requires monitoring clinical studies in phases II-III, ensuring adherence to GCP, and initiating investigator sites. Candidates should have a Bachelor's degree in life-science, a minimum of one year of relevant experience, and be fluent in both English and Italian. Strong communication skills are essential for success in this role. A full clean driver's license is also required.

Competenze

  • Minimum 1 year monitoring experience as CRA within a CRO, Pharma, Biotech.
  • Experience with site initiation and site close out.
  • Experience in clinical studies phase II-III.

Mansioni

  • Monitoring clinical studies in phases II-III.
  • Assuring adherence to Good Clinical Practices and compliance with study procedures.
  • Identification, qualification, and initiation of investigators and their sites.
  • Supervising study conduct according to GCP requirements.

Conoscenze

Monitoring clinical studies
Fluent English
Fluent Italian
Excellent communication skills

Formazione

Bachelor degree in life-science
Descrizione del lavoro
Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate in Italy

Job Overview
  • Monitoring clinical studies in phases II-III
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Identification, qualification and initiation of investigators and their sites.
  • Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
  • Bachelor degree in life-science
  • Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Italy
  • Experience in commercial studies
  • Experience with site initiation, site close out
  • Experience in clinical studies phase II-III
  • Fluent English & Italian
  • Excellent communication skills
  • A full clean drivers license
  • FTE: 1.0

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email info@life-science.co.uk

Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.