Dear Allstat,
Please find below the details for our latest contract Statistician role.
If this position is of interest to you please send an updated CV to
[log in to unmask] or alternatively you can reach me on +44 (0)207
922 7126
JOB DESCRIPTION
Our clients based in the South East are actively looking for an experienced
Contract Statistician to work full time on-site. This is a 12 month contract
initially with opportunities to extend.
-Primary aspect of the role is to work as lead statistician for a GI
project.
-Supporting phase I-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).
-You will work in a multi-functional environment and will need to be a good
communicator.
REQUIREMENTS
-Extensive experience gained in all main tasks of a Senior Statistician.
-Leadership skills & Project management skills.
-Knowledge of drug development process and relevant HA guidelines.
-Knowledge and expertise in statistics and its applications in clinical
trials.
Other key aspects MSc necessary (or equivalent experience); experience
communicating with regulatory authorities useful; experience managing work
at a CRO is preferable.
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