Senior/Clinical Document Specialist -£20k

Develop further your skills within clinical development support - if you don't want to be a CRA and are looking for the next step look no further! The Company: This global speciality pharmaceutical company reported revenues in 2004 of $1,363.2 million and an operating income of $446.4 million. The growth rates for revenues were up by 13% on the previous year. Specialising in the development of Aids/HIV, renal and psychiatry treatments the company focuses on targeted therapies and treatments for specific patient populations. The Job: This role is available at two levels - senior and specialist - depending on experience. The main focus of both roles is document management for clinical trials and the provision of admin support to development programmes. You will maintain complex and specialised clinical study files in house in accordance with relevant regulations as well as liaising with CROs and other vendors for the management of their files. You will set up tracking systems for relevant tasks, deliverables and documentation. In this job you will also train and mentor junior members of staff and eventually hold line management responsibility. The Person: What are we looking for? You know who you are - educated to degree level with two years clinical trial administration or document management experinence gained within the pharma or CRO environment. You will have had some mentoring experience and for the more senior position time spent in a supervisory or management role. This is an excellent opportunity to further your career in an office based support role! Call ASAP to find out more.

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