Our client, an international biopharmaceutical is seeking a contract
statistician for a long term assignment. Working as a support statistician
to the statistical lead, you will be involved in all aspects of statistical
sections of the clinical trails. This will include but be limited to:
• Collaborate in the preparation and review of clinical assessments.
• Provide statistically sound experimental design and data analysis input to
meet project objectives.
• Review all project protocols, author protocol statistical analysis
sections and generate study randomizations.
• Develop study analysis plans as a team member;
• Review case report forms to ensure that protocol objectives are met and
project standards are maintained.
• Develop statistical programs as necessary to perform analyses, prepare
data displays, and verify data accuracy and validity.
• Author statistical analysis results in the clinical study report.
In order to be considered, ideally you should have a Masters with 3 to 4
years clinical trail experience and be available to start in the next 2
months.
Competitive Rates!
Please contact Suzannah Austen-Adams at [log in to unmask] or + 44
1666 840 323 for further information.
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