SRG is seeking a Clinical Trials Associate in Hitchin, United Kingdom. The role involves managing Trial Master File activities, ensuring compliance with regulatory standards, and offering comprehensive support for clinical studies. Ideal candidates will have at least 2 years' experience in clinical trials, strong organisational skills, and an understanding of GCP regulations. You'll play a key role in high-quality trial delivery while working in a supportive environment. A driving license is preferred due to location considerations.
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