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 sponsor dedicated home based in Andalusia.
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
- Fluent English & Spanish
- Excellent communication skills
- A full clean drivers license
- FTE: 1.0