Senior Document Manager Associate- Leading Pharma
An opportunity with an international pharmaceutical company has arisen, dealing with Regulatory, Clinical and Preclinical document management. Working alongside various department on a global level, you will also liaise with CROs to ensure documents are ready for regulatory submission.
Based West of London, this is an excellent location away from the rat race in London. There is career options at this company, where you will be working globally with Document management.
You should have a strong background dealing with document management, regulatory, clinical studies and liaising with CROs. Knowledge of regulatory submission requirements is beneficial.
If you are interested get in touch with Jonathan McNab on +44 (0)207 940 2105 or email your CV in M.S Word format to email@example.com to find out more about this position, or any other similar positions we may have available!