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ALLSTAT  June 2010

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Subject:

Re: NEW JOBS: Head of Programming and others

From:

Justin Gimblett <[log in to unmask]>

Reply-To:

Justin Gimblett <[log in to unmask]>

Date:

Wed, 2 Jun 2010 15:58:17 +0100

Content-Type:

text/plain

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text/plain (1 lines)

Dear Allstat



We have a number of urgent roles we are trying to fill on behalf of clients: 



Head of Programming, Germany - Permanent - Salary to be confirmed

Lead a group of up to 10 programmers; develop a standardized data repository to support regulatory submissions, statistical analyses, PK/PD modeling, trial simulations and safety monitoring; input in the clinical project and study teams regarding biometrics programming activities and data applications as needed. 5-10 years prior pharma industry experience in a mathematics, statistics or programming role and strong leadership skills





Senior Statistician, Oncology, Switzerland - 6 months renewable contract, Up to 1000 CHF per day

Act as the lead for Biostatistics and Statistical Reporting activities within one or more drug programs in Oncology area; Responsible for all statistical input at the program level and for all statistical tasks of the assigned clinical studies e.g. clinical trial design/planning, analysis plan, reporting activities, support to publications, and any statistical consultation during the running phase; Promote and implement innovative approaches to study design and decision making; Track and resource project and clinical trial activities and milestones. Masters degree in Statistics (or similar)

with  significant experience or PhD in Statistics with some experience as a statistician or project statistician for international clinical teams;          Experience in Oncology Statistics and applied Bayesian methodology is highly desirable.





Senior Statistician, North England - 6-12 months contract

Working as study or project lead you will design clinical studies, provide statistical analysis to support risk assessment, perform statistical analysis and interpret results, support regulatory submissions. MSc required in mathematics or statistics subject, previous responsibility for study design and regulatory submissions, specialist knowledge of one or more therapeutic areas (e.g. clinical pharmacology, discovery medicine, health economics), project management skills.





Project Biostatistician, the Netherlands - Perm or contract available

Act as local or global project statistician, contribute to the clinical development plan, lead all statistical aspects for assigned studies including study design and reporting. Must have pharmaceutical or CRO experience. Advanced knowledge of SAS/Base and SAS/Stat programming and from 4-8 years of post MSc experience.





Statistician, Czech Republic - Perm or contract available

Minimum of 2 years prior pharmaceutical or CRO experience together with an MSc in Mathematics or Statistics related discipline. Input into all aspects of clinical trials from design to analysis and report writing.





Statistician, Germany - Perm or contract available

Responsible for all statistical aspects of clinical trials from design through to analysis and report writing. 3 years prior pharmaceutical or CRO experience together with an MSc in Mathematics or Statistics related discipline.





Senior Statistician, France - Permanent

3-5 years post Masters pharmaceutical industry experience is required. You will have full input into the statistical elements of the protocol document, carrying out the statistical analysis and writing the analysis plans for submission. You will also mentor more junior statisticians. Salary level according to experience.





Project Statistician, France - Permanent

Responsible for all statistical aspects of the clinical development project, define the project standards (phase II/III/IV) i.e. the statistical sections of the core protocol, the stats analysis plan with project analysis datasets and the definition of analyses; You will prepare final draft tables, graphs and listings for the CTD and are responsible for the interpretation of statistical results for submissions. You will also address statistical issues in the publication strategy and at meetings with regulatory agencies.





• Please note that applications are only invited from those candidates who are currently eligible to work in the EU as applicable, as sponsorship will not be provided for these roles.





If you are interested in any of these vacancies then please contact Key People:



Justin Gimblett  

Email: [log in to unmask] or telephone: +44(0)1727 817 617



Ilan Lynton

Email: [log in to unmask] or telephone: +44(0)1727 817 626



You can see our other vacancies at www.keypeople.co.uk  



Kind regards





Justin Gimblett

Recruitment Manager

 

Key People Ltd.

Catherine House / Adelaide Street / St. Albans / Herts. / AL3 5BA

 

Direct Tel: +44 (0)1727 817 617 (ddi) / Switchboard Tel: +44 (0)1727 811 634 / Fax: +44(0)1727 844 838

Email: [log in to unmask] 

LinkedIn Profile: www.linkedin.com/in/justingimblett 

Website: http://www.keypeople.co.uk 



Refer a friend and get paid



At Key People many of the people we place have been referred to us by their friends and colleagues. If you refer someone to our division and we are able to help them secure employment, then after successful completion of the probation period, we will reward your efforts with a 'thank you’ for up to £250 (or currency equivalent).









You may leave the list at any time by sending the command



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