If interested please contact Kien-Sen Lee at
[log in to unmask] or on the contact numbers given in the
job description. Please do not respond to this email address.
Dear Allstat,
Please find below the details of our latest Statstics contract
opportunity in Europe.
If this position is of interest to you please forward an updated CV to
[log in to unmask], for a private consultation contact me
directly on +44 207 922 7126
For all our latest Contract and Permanent vacancies please go to
www.hayspharma.com
JOB DESCRIPTION
My client is based in a beautiful country in Western Europe and are
looking for an experienced statistician to join them, they have a strong
pipeline coming up and are looking at the long term plans.
Due to a recent merger with a large Pharmaceutical they are looking to
expand their current SAS and Stats group.
There are a variety of TA's they currently work on although their core
focus are the Reproductive Health and CNS TA's.
They are currently interviewing candidates at the moment and are looking
for someone to start ASAP with rates negotiable depending on experience.
DUTIES
-Write detailed statistical analysis plans for clinical trials as well
as for integrated summaries of efficacy and safety.
-Analyse clinical trial data producing accurate results representing the
outcome of the trial.
-Validate statistical output.
-Accurately interpret and clearly communicate statistical results and
concepts to non-statisticians.
-Co-author final integrated reports of clinical trial data writing
thorough and clear statistical methods sections and producing the
statistical appendix for the reports.
-Provide statistical output as required for manuscripts and ensure that
the results are accurately interpreted in the publications.
-Provide input into statistical SOPs and general standardization efforts
within the department (e.g. statistical methodology standards, standard
data presentations).
-Participate in interactions with regulatory agencies as required.
-Collaborate effectively with members of clinical trial implementation
teams and with Biometrics colleagues.
QUALIFICATIONS
-Language and Education
-Fluency in English.
-Ph.D. or MSc in Statistics or Biostatistics or equivalent, with
extensive and broad pharmaceutical/ biotechnology
-experience.
-Professional Skills and Experience
-Working SAS knowledge and proficient in SAS statistical procedures.
-Knowledge of ICH statistical regulatory requirements.
-Personal Qualifications
-Interpersonal skills, initiative, creativity.
-Excellent communication skills.
Kien-Sen Lee
Consultant, Biostatistics - Hays Pharma
t. +44 (0) 20 7922 7126
f. +44 (0) 20 7922 7101
m.+44 (0) 7957 952775
Hays Pharma is part of the Hays Plc group of companies - for all our
latest jobs and industry news go to www.hayspharma.com.
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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privileged. If you are not the intended recipient, you should not disclose,
copy or use any part of it - please delete all copies immediately and notify
the Hays Pharma Helpdesk at [log in to unmask] .
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the author who
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Hays Pharma is a member of the Hays Plc group of companies. Hays Plc
is registered in
England and Wales, number 2150950. Registered office, 141 Moorgate, London
England, EC2M 6TX.
******************************************************************************
#####################################
James Miller
Department of Statistics
University of Glasgow
15 University Gardens
G12 8QQ
0141 3302474
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