Clinical Research Associate – Netherlands

Resourcing Life Science; Netherlands; On-site; EUR 40,000 - 60,000; Full time

Job summary

A global clinical research organization is seeking a CRA / Clinical Research Associate to monitor clinical studies in phases II-III in the Netherlands. The successful candidate will ensure adherence to Good Clinical Practices and manage site initiation and closeout. A Bachelor degree in life-science and at least 1 year of CRA experience in CRO, Pharma, or Biotech is required. Candidates must be fluent in English and Dutch, possess excellent communication skills, and hold a full clean driver’s license.

Qualifications

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

Responsibilities

• Monitor clinical studies in phases II-III.
• Ensure adherence to Good Clinical Practices and compliance with study procedures.
• Identify, qualify, and initiate investigators and their sites.
• Supervise study conduct according to GCP requirements.

Skills

Monitoring clinical studies

Excellent communication skills

Fluent in English

Fluent in Dutch

Education

Bachelor degree in life-science

Job description

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 Netherlands

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 Netherlands
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English & Dutch
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0