Clinical Research Associate in Portugal
3 semanas atrás
Company Overview
Our client is a leading Contract Research Organization (CRO) supporting various Pharmaceutical & Biotech companies globally.
Job Summary
We are seeking a skilled Clinical Research Associate to monitor clinical studies in phases II-III, ensuring adherence to Good Clinical Practices and investigator integrity.
Main Responsibilities
• Identify, qualify, and initiate investigators and their sites.
• Supervise study conduct according to GCP requirements and all applicable laws.
Requirements
• Bachelor degree in life sciences.
• At least 1.5 years of monitoring experience as a CRA in a CRO, Pharma, or Biotech setting in Portugal.
• Experience in commercial studies and site initiation/site close-out.
• Fluent English and Portuguese language skills.
• Excellent communication skills.
• Full clean driver's license.
What We Offer
A challenging role in a dynamic environment with opportunities for growth and development.
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