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Graduate Drug Safety Specialist - Cambridgeshire




Interested in a career with a global industry leading research organisation? Wanting to work within drug safety/ pharmacovigilance- a growth area of clinical research? We have Associate Safety Specialist opportunities within a global clinical contract research organisation (CRO). Working within the drug safety/ pharmacovigilance function you will be responsible for managing the serious adverse event (SAE) processes and the co-ordination of database activities. You will be required to maintain a knowledge and understanding of the organisation`s SOPs and WPDs in addition to current international regulations and guidelines relating to clinical trials, regulatory documents and safety issues. Successful candidates may either have a life sciences degree (e.g. Pharmacology, Biology), medical qualifications (GMC registration not required) or have nursing qualifications. Experience working within a clinical research or medical environment would be advantageous. Strong communication and teamworking skills are required along with an excellent level of attention to detail and accuracy in your work. Interested? Call Andy on 0131 473 2343 or email a copy of your CV to andy@squarepegs.biz


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