Dear Allstaters,
Please find below, brief details of 4 new contract vacancies for you to
review....
TITLE: SAS PROGRAMMER - EARLY STAGE CLINICAL DEVELOPMENT Essential, educated
to degree level or equivalent, minimum of 2 years SAS programming within the
pharmaceutical / CRO environment, SAS/base, SAS/macro, SAS/stat,
PROC/Report, experience of reporting early development clinical trials,
knowledge of statistical methodology used to report clinical trials &
knowledge of reporting pharmacokinetic data. Desirable, SAS/Graph OR
SAS/SQL. Working for this major pharmaceutical client this role involves the
production and quality of data presentations / analyses for various clinical
trials conducted in extracting data into in house early development. Your
duties will include; extracting data into the in-house reporting systems,
writing / validating software according to statistical analysis plans,
assess quality of all outputs, producing tables / listings / figures /
datasets, identify reporting issues & resolve. INTERVIEW TIMES AWAIT.
LOCATION - Belgium
CONTRACT LENGTH - 6 months+
____________________________
TITLE: SAS PROGRAMMER - PHASE I-IV DIAGNOSTIC TRIALS Essential, 3-4 years
minimum SAS programming within the Pharmaceutical / CRO industries,
SAS/base, SAS/macro, SAS/graph & excellent reporting experience. Desirable,
an understanding of statistics OR any specific therapeutic knowledge of
diagnostics. Working for this major client in various study teams, you main
duties will be to program high quality tables, listings & summaries.
INTERVIEW TIMES AWAIT.
LOCATION - GERMANY
CONTRACT LENGTH - 6 months+
____________________________
TITLE: SAS PROGRAMMER - FDA SUBMISSION PROJECT Essential, 2 / 3 years
minimum statistical SAS programming within the pharmaceutical / CRO sectors,
SAS/base, SAS/macro, statistical knowledge (although no formal qualification
needed) & fluent in English. Desirable, SAS/stat & a command of the French
language. Working with this pharmaceutical client you be working on a phase
II-III FDA submission project. Your duties will include; interpreting data
from statistical analysis plans and producing tables / summaries / listings.
INTERVIEW TIMES AWAIT.
LOCATION - NETHERLANDS
CONTRACT LENGTH - 12 months
____________________________
TITLE: STATISTICAL PROGRAMMER - SAFETY / EFFICACY SPECIALIST Essential;
educated to degree level or equivalent, 3 years SAS / Statistical
programming experience within the pharmaceutical / CRO industry, 3 yrs
SAS/base, 3yrs SAS/Macro, 3yrs PROC/Report, study reporting experience,
excellent knowledge of efficacy reporting & an understanding of statistics.
Working for this major pharmaceutical client, you will be producing efficacy
& safety reports on there phase IV clinical trials. Your duties will
include; production / QC of efficacy study reports in SAS, writing /
validating software in accordance with statistical analysis plans &
production / QC of safety study tables / listings. INTERVIEW TIMES AWAIT.
LOCATION - SPAIN
CONTRACT LENGTH - 3 months
____________________________
If you are interested in any of these positions, please feel free to get in
contact. However, if you are not available, please feel free to forward my
details on.
Regards
James Carrera
European Contracts Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Mobile: +44 7717 578 246
Fax: +44 (0) 207 255 6656
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www.1st-pharmapeople.com <http://www.1st-pharmapeople.com/>
PLEASE NOTE: As of 31st May 2005 our office address will change to; 1st IT
People, 3rd Floor, Woolverstone House, 61-62 Berners Street, London. W1T
3NJ. As a result of this, we do have a new telephone number of 0207 255
6665. Please note our previous phone number will still work.
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