Senior Medical Writer - £35k

Join a market leader offering excellent training opportunities to medical writers! This company conducts phase I-IV clinical trials on a global level for blue chip pharma and biotech companies. Due to recent reorganisation within the regulatory services group an opportunity exists for an experienced medical writer to join the established team based in Berkshire. The job will involve writing a variety of clinical documents from protocols and study reports through to high level regulatory documentation. This is also a consulting role where you will provide advice to clients on the production of these documents. Process improvement is also a key part of this role and you will develop and implement ideas to improve the efficiency of the department. We are looking for candidates with 3-5 years experience preparing clinical documentation - in particular clinical study reports. Applications are welcomed from experienced project managers interested in medical writing if they are able to demonstrate experience writing documents. Excellent benefits are available in addition to the chance to work on some of the largest studies in the industry! If you are interested please call for more details.