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Our client is an AIM listed pharmaceutical group developing a portfolio of prescription medicines derived from cannabis to meet patient needs in a wide range of therapeutic indications. Working closely with officials from the Home Office, they maintain control over all aspects of the product development process - botanical research, cultivation, extraction, formulation into drug delivery technologies, clinical trials and regulatory affairs. They are now looking to recruit a Regulatory Affairs Project Manager to join the team at their Wiltshire office where the number of projects and countries covered is rapidly expanding. The successful candidate will possess a life science degree, have 3-4 years experience in Regulatory Affairs, have good verbal and written communication skills and enjoy working both in a team and independently. Ideally, the candidate will also have particular experience in clinical issues and in the Mutual Recognition Procedure. All aspects of Regulatory Affairs through from Clinical Trials Applications, preparation of all Modules of the Common Technical Document, submission of variations and an International dimension will be in store. Skill in interacting with colleagues throughout the company on different sites, and co-ordinating timely submissions to the Authorities will be required.
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