Dear Allstat,
Please find below our latest CONTRACT Stats Programming role. The
contract is due to start in May for 6 months initially.
My client is actively looking for a Statistical Programmer with a
minimum of 3-4 years experience within the pharmaceutical field
Duties and Responsibilities:
- Provide programming support and validation of analysis data sets,
pooled datasets, statistical summary tables, figures and patient data
listings for phase I - phase III clinical trials, ISS & ISE, primarily
using SAS.
- Provide output for the Clinical Study Report, the Integrated Summary
of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic
submissions.
- Need for ensuring standardization of programs where applicable.
- Apply knowledge of clinical data, the design and phases of clinical
trials, statistics, relevant regulations and the pharmaceutical industry
to the implementation of tasks.
- Handle complex statistical programming issues independently and be
familiar with study programming issues. Bring ideas for new projects and
take the initiative to solve issues.
Please forward your CV for an immediate review. We have telephone
interview slots for next week.
Kind Regards
Mark O'Brien
Consultant ~ Clinical & Biometrics
James Harvard Pharmaceutical Ltd
T. 020 7922 7106 M. 07921 176225 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
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