Clinical Research Associate Regional Monitoring
hace 2 semanas
Job Title: Regional Monitoring Clinical Research Associate
Company Description:
Our client is a global Contract Research Organization (CRO) that provides comprehensive services to pharmaceutical and biotechnology companies worldwide. They offer a full-service solution encompassing clinical and non-clinical development, peri-approval, and market access.
Job Overview:
As a Regional Monitoring Clinical Research Associate, you will be responsible for monitoring clinical studies in phases II-III, ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. You will identify, qualify, and initiate investigators and their sites, and supervise study conduct according to GCP requirements and all applicable laws.
Key Responsibilities:
- Monitoring clinical studies in phases II-III
- Ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures
- Identifying, qualifying, and initiating investigators and their sites
- Supervising study conduct according to GCP requirements and all applicable laws
Requirements:
- Bachelor's degree in life sciences
- Minimum 1 year of monitoring experience as a CRA within a CRO, Pharma, or Biotech in the Netherlands
- Experience in commercial studies
- Experience with site initiation and site close-out
- Experience in clinical studies phase II-III
- Fluent in English and Spanish
- Excellent communication skills
- A full clean driver's license
About Us:
Our client is a global leader in the CRO industry, with a strong presence in the pharmaceutical and biotechnology sectors. They offer a dynamic and challenging work environment, with opportunities for professional growth and development.
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