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ALLSTAT  2004

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Subject:

Vacancy / Reporting Statistician for Phase IV Projects

From:

Angie Farrell <[log in to unmask]>

Reply-To:

[log in to unmask]

Date:

Wed, 22 Sep 2004 09:01:19 +0100

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (57 lines)

*** PLEASE NOTE THIS VACANCY IS BASED IN MADRID  FOR 6 MONTHS INITIALLY***

This job involves production of efficacy and safety study reports for
Phase IV Clinical trials in Spain.  This role involves 2 main areas:
- The production of quality control of efficacy study reports written in
SAS.  This is achieved by writing and validating software in accordance
with statistical analysis plans.
- The production and quality control of safety study tables and listings
created by running software within current existing reporting tools.

Both roles would require identification of the general cause of any
reporting issues (e.g. data or programs) and their possible resolution
with data management, programming, statistical or clinical staff as
appropriate.

Essential Criteria

3+ years of SAS/BASE
3+ years of SAS/Macro
3+years of PROC REPORT
- Experience of Pharmaceutical data and reporting clinical trials.
- Experience of working closely with a study statistician to discuss and
produce efficacy study reports
- Good time management and planning skills

Interested?  Please send your updated CV with a short cover note to
[log in to unmask]


Kind Regards

Angie Farrell
Resourcing Manager
Chiltern International Limited
171 Bath Road
Slough
Berkshire SL1 4AA
United Kingdom

Direct Line: +44 (0) 1753 216744
Mobile: +44 (0) 778 6982644
Fax: +44 (0) 1753 511116
Website www.chiltern.com

______________________________________

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