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ALLSTAT  2004

ALLSTAT 2004

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Subject:

JOB - Manager, Clinical Statistics Endocrinology - Mid-size Pharma Company - Berkshire UK or Paris France

From:

James Brooks <[log in to unmask]>

Reply-To:

James Brooks <[log in to unmask]>

Date:

Fri, 8 Oct 2004 11:30:31 +0200

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (56 lines)

Dear allstat list members,

I am a researcher for Euromedica, an executive search company specialised in
the healthcare field. I am working on an assignment to recruit a MANAGER
CLINICAL STATISTICS - ENDOCRINOLOGY for a well-respected and successful
pharmaceutical company, with the position being based in either Paris or
Berkshire in the UK, depending on the choice of the successful candidate.
Experience in endocrinology is not a 'must' for this position but experience
of FDA procedures is. An abridged version of the announcement for this
project runs as follows;

COMPANY: Our client is a mid-sized pharmaceutical company that has enjoyed
considerable sustained growth over the last decade(pharmaceutical sales have
more than doubled) thanks to their commitment to R&D. The group has over 20
products on the market and a strong international presence. Endocrinology is
represented by treatments for acromegaly and neuroendocrine tumors.
Innovative new formulations of these medicines have entered clinical
development.

APPOINTMENT: With their programmes gaining ground our client now requires a
Clinical Statistics Manager in Endocrinology. This person will ensure that
the clinical projects are conducted according to an appropriately rigorous
statistical approach. The incumbent will design, implement and report
statistical processes in clinical trials and present those statistical
methods used to the Regulatory bodies when required. He/ she will also
evaluate and oversee the statistical capabilities of any contracted CROs.

IDEAL CANDIDATE: *A science degree with additional qualification in
statistics. *Minimum of 5 years drug development experience within a
pharmaceutical company or CRO. *Experience dealing with FDA procedures is
essential. *Excellent communication skills in English. *Good understanding
of GCP and ICH guidelines. *Experience of working within multi-disciplinary
teams. *Mobility: the position is primarily office-based but travel both
within Europe and US will be necessary.

Please don't hesitate to contact me for more information (details below) or
just a discussion in confidence. Of course, any help which any of you can
provide in forwarding these details to contacts not subscribed to allstat
who you think could be interested would be greatly appreciated.

Many thanks,

James

James Brooks
Principal Research Associate

EUROMEDICA
165 Boulevard Haussmann
75008 Paris, France
Tel: +33 (0)1 49 53 57 09
Fax: +33 (0)1 49 53 05 44
E-mail: [log in to unmask]

Website: www.euromedica.com

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