As a Clinical Research Associate (CRA) will be working on critical clinical trials for large, prominent pharmaceutical companies. As a CRA, you will conduct site monitoring responsibilities for Clinical trials, according to Company Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring and Close-out visits.
Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets
- Training and development, both initially and throughout your career
- Join a company where people tend to stay for 6-10 years rather than 1-3!
- Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.