Dear Allstat,
Please find below a brief job description for 2 contract requirements
with a global pharmaceutical company based in the South of England. The
requirement is for Senior Statistical Programmers with a minimum of 3
years pharmaceutical or CRO experience.
Key Skills:
Demonstrated ability to lead programming aspects of a clinical trial
Expert knowledge of SAS, including SAS BASE, Macro, Report, familiarity
with SAS Graph, ODS and SQL desired
Experience of involvement in project level programming activities
(pooling of data for ISS, ISE), electronic submission
Good knowledge of clinical trials, statistics
Good knowledge of ICH GCP issues as they affect reporting
Fluent in Enlgish
Minimum a BA/BS University degree in Computer Science, Statistics or
related scientific field
Responsibilities:
Responsible for the input into specifications for analysis (including
derived datasets, listings, tables, graphs) of clinical trials across
Phase II-IV and for project deliverables (SCS and SCE)
Subsequent timely delivery of high quality tables, listings and graphs
of clinical trials and project deliverables from analysis plan,
including ad-hoc exploratory analyses
Represent line function within clinical teams
Ensure that documents and specifications are consistent and comply with
company standards
If you would like to find out more about these vacancies, please contact
me directly to discuss the roles in confidence.
Kind Regards,
Chris Smith
Consultant ~ Clinical and Biometrics
James Harvard Pharmaceutical Ltd
T. 020 7922 7137 M. 07919 448334 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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