If interested please contact Chris Smith at
[log in to unmask] or on the contact numbers given in the job
description.
Dear Allstat,
Please find below the details of our latest Contract vacancy based in
Mainland Europe. This is an extendable 6 month contract offering
outstanding rates with subsidised accommodation.
SENIOR OR PRINCIPAL BIOSTATISTICIAN
PURPOSE OF THE ROLE
May manage a small number of Biostatisticians and/or statistical
programmers focused
on a limited number of Therapeutic areas. With limited direction,
provide statistical input
for statistically complex protocol development. With limited direction,
write statistical
analysis plans & perform statistical analyse for statistically complex
clinical trials.
Independently provide statistical input for statistically routine
protocol
development. Independently write statistical analysis plans and perform
statistical
analysis for statistically routine clinical trials. With limited
direction, participate in
departmental standardization efforts.
KEY TASKS & RESPONSIBILITIES
* Statistically mentor Biostatisticians and programmers in relevant
therapeutic areas
* Keep abreast of statistical developments
* Research and write statistical conventions
* Develop statistical standards for clinical development programs
* Validate tables & derived listings as required
* Ensure that programming and validation is performed
* Independently provide statistical input for statistically routine
protocol/CRF
development and query checks
* Write analysis plans for statistically routine clinical trials
* Write analysis plans for statistically complex trials as well as for
integrated safety
& efficacy summaries
* Analysis plan written include the most appropriate statistical
methodology & data
presentations
* Review analysis plans for statistically routine clinical trials
* Analyze statistically complex clinical trials
* Review analysis results for statistically routine clinical trials
* Write accurate, logical, clear, concise, thorough & objective
statistical methods
sections for statistically routine integrated final reports
* Review statistically integrated draft reports ensuring the accuracy of
the statistics
as well as their interpretation
* Review statistical method sections & the interpretation of results
written for
statistically routine clinical trials
* Independently perform routine statistical analyses for manuscripts
* Perform complex statistical analyses for manuscripts
* Review manuscripts, perform complex statistical analyses for
manuscripts
* Review manuscripts for accurate statistic & statistical interpretation
* Understand manuscripts for accurate statistical interpretation
* Understand & follow all statistical programming SOPs as well as any
other
relevant SOP
* Write statistical SOPs as required
* Review statistical & statistical programming SOPs
* Provide input into general standardization efforts
* Develop routine 6 complex statistical standards
* Provide direction to biostatisticians & statistical programmers in the
standardization area
* Provide input into the determination of the AOP for the department as
required
* Provide leadership to non-statistical colleagues with statistical
issues
* Lead process improvement teams as required
EDUCATION/LANGUAGES
* PhD or MSc
* English fluency
PROFESSIONAL SKILLS & EXPERIENCE
* 5 - 8 years pharmaceutical/Biotech experience
* SAS experience & highly proficient in SAS statistical procedures
* Extensive knowledge routine statistical methodology
* Fundamental knowledge of relevant clinical areas
* Knowledge of the statistical & clinical regulatory
guidelines/requirements specific
to relevant therapeutic areas & their implications for statistical
analysis
PERSONAL SKILLS & COMPETENCIES
* Excellent communication skills
* Self directed
* Exhibits initiative & sensitivity in conflict resolution
* Recognized as a problem solver who focuses on facts
* Consistently makes informed decisions seeking guidance if necessary
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 www.hayspharma.com
I look forward to hearing from you.
Kind Regards,
Chris Smith
Senior Consultant, Biostatistics - Hays Pharma
t. +44 (0) 20 7922 7137
f. +44 (0) 20 7922 7101
m.+44 (0) 7919 448334
Hays Pharma is part of the Hays Plc group of companies - for all our
latest jobs and industry news go to www.hayspharma.com.
P Please consider the environment before printing this e-mail
Hays Pharma is proud to be a Carbon Neutral Company
http://www.carbonneutral.com/
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Hays Pharma is a member of the Hays Plc group of companies. Hays Plc
is registered in
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******************************************************************************
#####################################
James Miller
Department of Statistics
University of Glasgow
15 University Gardens
G12 8QQ
0141 3302474
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