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This is a senior regulatory affairs role with a market leader! This global company has a large clinical development group with more depth of therapeutic expertise and a broader range of services than any other provider! In this role you will provide both scientific and regulatory expertise regarding preclinical and clinical aspects of drug development for drugs and biological products. This is a highly strategic role in which you will work with blue chip companies to guide them through the regulatory process with the FDA, EMEA and other local country authorities for the development of drugs and biological products - this includes due diligence evaluations and in-out licensing activities. You will also be highly involved in supporting business development activities, giving presentations on the regulatory capability and expertise of the company. This is a highly commercial role in which you have significant impact on regulatory strategy both internally and externally. There is lots of scope for further development with this company, either into a global regulatory role which will be more strategic or into line management. There is no ceiling in this company so your opportunities for progression will be endless! We are looking for candidates with extensive regulatory experience in clinical development. It is essential that you have knowledge of the FDA and EMEA requirements for developing drugs and biological products - this experience can come from either a pharma company, CRO or regulatory authority. Knowledge of the European regulatory processes and requirements is essential. Your experience will cover phases I-IV of development and you must have highly developed communication skills. If you think youve got what it takes to be in a high profile role with one of the worlds largest development services companies give us a call to find out more!