Introduction

An exciting opportunity has arisen to work for a cutting edge clinical stage therapy company who aim to develop treatments for serious diseases

You will be responsible for:

• Reviewing and approving nonclinical study documentation including study protocols and study reports of non-clinical studies
• Managing the preclinical department documentation storage and retention
• Aiding internal audits of non-clinical studies
• Proposing the implementation of continuous improvement programmes
• Assuring data integrity and compliance with pre-clinical policies

You will be bring:

• A BSc in a scientific discipline
• 1 year of experience working in QC or a non-clinical study environment
• Experience with quality documentation review and approval
• Proficiency in Microsoft office

If you want to be part of an innovative company where you can grow and expand your current knowledge, GET IN TOUCH by emailing me on isaac.murray@biotalent.com