Clinical Research Associate Regional Monitoring in Madrid Position
hace 2 días
**Job Overview**
As a Clinical Research Associate Regional Monitoring, 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.
**Key Responsibilities:**
- Identify, qualify, and initiate investigators and their sites
- Supervise study conduct according to GCP requirements and all applicable laws
- Ensure adherence to Good Clinical Practices and investigator integrity
- Comply with all study procedures
**Requirements:**
- Bachelor degree in life-science
- Minimum 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Netherlands
- Experience in commercial studies
- Experience with site initiation and site close out
- Experience in clinical studies phase II-III
- Fluent in English & Spanish
- Excellent communication skills
- Clean driver's license
**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.
**About Us:**
We are Resourcing Life Science, a recruitment agency dedicated to providing top talent to the life science industry.
**Why Work with Us:**
At Resourcing Life Science, we pride ourselves on building long-term relationships with our clients and candidates. We offer a unique approach to recruitment, combining industry expertise with a personalized service.
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