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Chintu
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In the complex world of drug development, inVentiv Health clinical is exactly where you need to be. With offices in more than 30 countries around the world, inVentiv Health clinical has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. inVentiv Health clinical works for you on trials of any size, anywhere around the world.
Working in partnership with our client Boehringer Ingelheim, this unique role plays a key part in the continual support of one of our Functional Strategic Partnerships. As such we are able to offer all the advantages of working for a top-five CRO combined with the benefits of operating as an integrated member of a multi-functional client-specific clinical team.
We have an exciting opportunity for a statistician to work in a small team within a team, dedicated to two key areas for our client:
• Exploratory research into the effect of biological and genetic markers on therapeutic response in late phase clinical trials
• Early phase clinical trials investigating pharmacokinetics, pharmacodynamics and early safety signals
This role would suit someone with strong SAS skills currently working as a programmer in the pharmaceutical industry who would like to make the move into a more statistical role or a statistician from another area of medical research with an interest in drug development. We will also consider applications from recent Masters graduates, again who have used SAS and have some relevant work experience.
You will be responsible for:
• Contributing to formal Statistical Analysis Plans.
• Performing statistical analyses of data and interpreting results to ensure validity of conclusions.
• Developing SAS programs as assigned, for current clinical studies.
• Interaction with
o Our sponsor client regarding scope of work and scientific context as well as monitoring of progress
o The Data Management function to ensure that datasets are in usable format and to perform statistical diagnostics prior to database locking.
o Medical writers in production of statistical and integrated clinical/statistical reports and other documents containing statistical information.
o Other departments, such as Clinical Operations and Project Management, to ensure a high level of client satisfaction through successful execution of projects.
And be able to meet the following requirements:
• A Bachelors degree, preferably a Masters, in statistics
• The ability to make a positive contribution within a team-oriented environment.
• Strong SAS programming skills in dataset preparation, data presentation and inferential analyses
• Be able to perform statistical analysis of clinical data:
o From early phase clinical trials with quick turnover
o In a data-driven, exploratory environment without needing detailed specifications
• Ability to read, analyse, and interpret common scientific and technical journals.
In return you can expect:
• The flexibility to be office or part home/office based.
• A competitive remuneration package with excellent benefits including, free parking, healthcare, pension, annual performance bonus and more.
• A commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organisation.
• The opportunity to work within a successful and rewarding environment.
We look forward to receiving your application
To apply or for more details please contact Frances Wells on +44 (0) 1628 408444 or email [log in to unmask]
Frances Wells
Senior Recruiter, EMEA
i3 International (UK) Limited
Star House, 20 Grenfell Road,
Maidenhead, Berkshire, SL6 1EH
T 01628 408444
F 01628 408428
M 44 (0) 7891182660
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http://www.inventivhealthclinical.com
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