Reference: 05503 Job Type: Permanent Date Posted: 11 August 2016
Job Type: Permanent
Date Posted: 11 August 2016
Our client, a global drug development firm, is looking for a Manager for their Drug Safety Services department to work in their Maidenhead office. Managing the overall Clinical Safety operations associated with products you will be working with various departments within the company, as well as external bodies including those concerned with Drug Safety and Regulatory affairs. You will have responsibility for the adverse events process, including data collected from clinical trials and reviewing patient narratives. This must all be accurately recorded, as you will be expected to participate in audits and report on a regular basis to clients and monitoring boards. With experience in the pharmaceutical, biotechnology or CRO industry you should have line management and / or project management knowledge. You will be able to interact with staff on both a functional and tactical level. An understanding of worldwide regulations and guidelines would be beneficial, as would knowledge of ICH GCP guidelines. There will be some travel involved and an extra language would be of use. In return our client offers a generous salary and full benefits package. If you would like to apply for, or learn more, about this diverse role please apply through this website.
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