Clinical Trial Regulatory Affairs Consultant

Clinical Trial Regulatory Affairs Consultant
Joining a highly successful regulatory affairs team, you will be expected to utilise your knowledge and expertise on regulatory requirements/legislation and liaise with different regulatory bodies including the EMEA & FDA.

The successful applicant will be responsible for advising and preparing clinical trial applications, post-marketing documentation and writing documentation for market applications of investigational medicinal products.

The ideal candidate will be degree educated in Pharmacy, Medicine or Science related discipline with regulatory affairs experience within a pharmaceutical environment. It is essential that you have prior knowledge of ICH and EMEA guidelines alongside reviewing and evaluating CMC, Pre-Clinical and Clinical data
In return you will receive a fantastic salary and benefits package including flexible working hours and much more.

For more information please call Kieron McDaid on 0121 616 3461

Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.