Dear Allstat,
Below are the details of our latest contract position bast in the South
East of England:
Purpose of Job:
* The Study Statistician/Programmer is a member of the clinical
team and is responsible for statistical/programming input to the
reporting of clinical studies.
* The Study Statistician/Programmer must ensure that activities
and processes performed are conducted according to company requirements.
This position works closely with other team members.
Major Responsibilities
* Act as a representative Statistician/Programmer on study teams,
managing your time so as to provide timely input.
* SAS programming to support the Statistical reporting, including
production of listing, tables and figures, for Phase II and Phase III
clinical studies and Pharmacovigilence data.
* Program/perform statistical analyses of data.
* Statisticians will be required to interpret analysis results,
ensuring validity of conclusions.
* Perform quality control review of study results.
* Act as a statistical/programming contact.
* Interact with Data Management personnel as necessary to ensure
that the data are in usable format; perform appropriate diagnostics
prior to database locking.
* Interact with report writers in the production of integrated
clinical reports and other documents containing information from
clinical study databases.
* Explore data for product profiling, hypothesis generation, new
research topics and publications.
* Input into the development of departmental processes, including
standard working practices and operating procedures.
Qualifications and Skills:
* A relevant Batchelors or Masters degree required.
* 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.
* Have a good understanding of clinical data, including data
quality issues.
* This position holder must be able to work without close
supervision. Well-developed time management skills are important.
* Able to work in a fast-paced, team-oriented environment.
* Possess excellent interpersonal and communication skills
(written and verbal).
* Strong attention to detail with a view to bring studies to a
quality conclusion.
* Flexible, positive, creative thinker, good communicator.
If you would like to discuss this position in detail, or for a
confidential consultation on all of our current Biostatistics and
Programming opportunities in the UK and Europe, please contact me
directly. Details of our current contract and permanent vacancies can
also be found at: http://www.jamesharvard.com/pharma/careers_browse.htm.
I look forward to hearing from you.
Kind Regards,
Chris Smith
Consultant ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. +44 (0)20 7922 7137 M. +44 (0)7919 448334 F. +44 (0)20 7922
7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
For the latest Statistics and SAS Programming vacancies go to
http://www.jamesharvard.com/pharma/careers_browse.php
We are exhibiting at the 2006 annual PhUSE Conference in Dublin between
October 9th-11th. Please come and see us at our stand.
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