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Introduction
Our client aims to improve the health, quality of life and well-being of patients throughout the world. They do this through our innovative range of diagnostic and pharmaceutical products that focus on the needs of individuals. Thiscompany is at the forefront ofthe fight against cancer and they have one of the world's most well known treatments for flu.

Summary of duties
As a project manager in this UK affiliate, you will be part of the Medical Affairs team, and will be one^of a team of dedicated CPMs and CTAs which provides medical expertise and advice to the business and customers.

You will co-ordinate the planning, conduct and follow up of clinical trials of both marketed products and those nearing the market. There will be the opportunity to get involved at study start-up as you work with medical advisors and brand managers to contribute to the development of local clinical trial strategies.

You will then help to plan those trials - contributing to protocols as well as organising all aspects of the clinical project management of the programmes and publication plans.

You will manage resources and budgets to ensure that projects deliver results on time and to budget. You will work closely with investigators and others to support the delivery of presentations and publications to raise awareness of trial results.

Qualifications required
Life Science, Nursing or Pharmacy degree or equivalent
Previous experience of monitoring clinical trials^in the UK
Previous experience of managing clinical trials, ideally in a pharmaceutical company in the UK
Excellent knowledge of ICH GCP and the EU Clinical Trials Directive
Strong interpersonal skills and team working skills