New Senior Document Management Role- Strategic Level
An international pharmaceutical company, investing heavily in Research and Development are recruiting a Senior Document Management position, dealing with developing and implementing the strategy for a new QC system for all global regulatory submissions. You will be dealing heavily with outsourced studies in this interested role managing full-life cycle regulatory submissions.
This is based in Hampshire, in an excellent location with a high standard of living- which is commutable from the centre of London. This is a permanent position in a new area of the business, which has been continuously expanding over recent months.
You should have strong knowledge of Regulatory submissions (ideally internationally through the EU and USA), dealing with document management and leading projects. A strong scientific understanding within preclinical areas such as DMPK, Toxicology, Pharmacology and Biological sciences required for this role.
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!