Our client is a well respected full service UK CRO. There is a lot of opportunity for advancement and development. They require a Statistician to join their small statistics team to carry out the design, analysis and reporting of clinical studies for all phases of clinical trials.
Experience with programming, analysis, and reporting in SAS is essential
Preious Phase I/II or multinational Phase III study work experience required.
International regulatory filing experience or Previous PK/PD Analysis experience would be an advantage
Training will be given for those statisticians at an early part of their career who show real promise
You must be qualified to MSC level in a mathematics or statistics related subject and have at least 1 year's prior pharmaceutical industry statistics experience.
Salary range £30 - £40,000 plus benefits, dependant on experience.
* Responsible for all aspects of clinical trial data analysis from statistical analysis plans and randomisations through to summary and analysis and direct input into clinical trial reports.
* Provide a flexible, expert consultancy service on all aspects of statistics within the clinical trials arena.
* Author and review Statistical Analysis Plans, including preparation of table shells
* Program in SAS all hypothesis tests and tables/figures/listings as necessary to meet project standards and timelines.
* Provide input into proposals and track study budgets as requested.
* Provide consultancy on investigator led studies and publications.
If interested please email your CV to Justin Gimblett at Key People: Email: [log in to unmask]
Or telephone +44 (0)1727 817 617 for more details
LinkedIn Profile: www.linkedin.com/in/justingimblett
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