Dear Allstat,
Please find below our latest CONTRACT vacancy in the UK.
My client is looking to recruit an additional Study Statistician or
Programmer to join their team initially on a 8 month contract
The successful candidate will be responsible for the
statistical/programming input into the reporting of clinical studies and
will work closely with other team members as well as ensuring that
activities and processes are performed in accordance with Company
requirements and SOPs.
Main Responsibilities:
Provide Statistician/Programmer input on study teams, managing your time
so as to provide timely input.
Provide SAS programming to support the Statistical reporting function,
including the production of listings, tables and figures for Phase II
and Phase III clinical studies.
Program/perform statistical analyses of data.
Interpretation of analysis results and ensuring validity of conclusions.
Perform quality control review of study results.
Act as a statistical/programming contact within the company
Qualifications and Skills:
A relevant Batchelors or Masters degree, with at least three years of
relevant pharmaceutical experience.
Good knowledge of applicable regulatory requirements and guidelines,
e.g. ICH Guidelines.
Proficient in the use of computers using the Windows Operating System
and Microsoft Office products.
A high level of computer proficiency, including SAS programming ability,
is required.
If your profile matches the job description please contact me to discuss
the role immediately. Excellent Rates
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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