Clinical Research Associate Regional Monitoring in Madrid Position

hace 2 días


Madrid, Madrid, España Resourcing Life Science A tiempo completo

**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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