*********** Wanted ***************
Contract biostatistician for immediate start.
The contract will run until end of 2007, and likely be renewed for 12
months.
The role is strictly based in-house in Hampshire, 5 days, 37.5hrs/week.
Ideally, candidates will have pharma experience supporting products at
post-approval phase.
Primary aspect of the role is to work as lead statistician for an approved
renal product which has just been launched in Europe, supporting phase
IIIb/IV activities, including; post approval commitments (ongoing clinical
studies outsourced to CROs), manage/perform regulatory requests for
additional safety analyses (there is some programming involved, including
working with a support programmer), manage statistical aspects of
publication planning (including additional analyses of existing clinical
trial databases).
This person will work in a multi-functional environment and will need to
be a good communicator.
Other key aspects: MSc necessary; experience communicating with regulatory
authorities useful; experience managing work at a CRO is preferable.
Are you this person? or do you know them?
If so, please send your CV ASAP to-
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