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CRA Portugal – Multi Sponsor

Resourcing Life Science

Lisboa

Presencial

EUR 30 000 - 50 000

Tempo integral

Há 23 dias

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Resumo da oferta

A global clinical research organization is seeking a Clinical Research Associate in Lisbon, Portugal. This role involves monitoring clinical studies, ensuring compliance with GCP, and working closely with investigators. Candidates should have at least 1.5 years of relevant experience and a Bachelor in life-science. Fluent communication in English and Portuguese is required.

Qualificações

  • Minimum 1.5 years of monitoring experience as CRA within a CRO, Pharma, or Biotech in Portugal.
  • Experience in commercial studies.
  • Experience with site initiation and site closure.

Responsabilidades

  • Monitoring clinical studies in phases II-III.
  • Assuring adherence to Good Clinical Practices and study procedures.
  • Supervising study conduct according to GCP requirements.

Conhecimentos

Monitoring clinical studies
Fluent English
Fluent Portuguese
Excellent communication skills
Site initiation and closing

Formação académica

Bachelor degree in life-science
Descrição da oferta de emprego
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 Clinical Research Associate in Portugal.

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 1.5 year monitoring experience as CRA within a CRO, Pharma, Biotech in Portugal
  • Experience in commercial studies
  • Experience with site initiation, site close out
  • Experience in clinical studies phase II-III
  • Fluent English & Portuguese
  • Excellent communication skills
  • A full clean drivers license
  • FTE: 1.0
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