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This is an exciting opportunity for candidates with an background in quality assurance and computer systems validation to join the leading provider of integrated data management solutions for clinical trials and drug safety.
You will be involved in a range of activities to ensure that processes and deliverables meet the expectations of customers, regulatory bodies and management. They will participate in and conduct customer and supplier audits and will be expected to provide regulatory consulting services and relevant training to internal staff across the International regions.
To be successful you will have a strong pharmaceutical background in either computer systems validation or clinical quality assurance. Experience of conducting internal and external audits, especially of hardware/software vendors, is highly sought after. You will be expected to have a thorough knowledge of key regulations and guidelines for clinical research and computerised systems.
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