If interested please contact Chris Smith at
[log in to unmask] or on +44 (0) 20 7922 7137. Please do not
respond to this email address.
Dear Allstat,
2 Biostatisticians urgently required for exciting projects based in
mainland Europe, with a top tier Pharmaceutical. Superb rates and
renewable contracts.
1 - Consultant - 1 year contract - Task: Phase 1 trial statistician
Background information:
The candidate will work in our Phase1_2a biostatistics team (5
Statisticians) and be responsible for planning and analysing Clinical
Pharmacology studies. Typical study types are Bioequivalence ,
Bioavailability (Drug drug Interaction, Drug Food Interaction, Drug
Formulation BA studies), Single Rising Dose, Multiple Rising Dose etc.
Scope of work:
The candidate will act as a fully responsible trial statistician.
He/she will collaborate with the Clinical Pharmacologist, Clinical
Kineticist, Data Manager and SAS Programmer. For non-complex trials, the
analysis and reporting may be contracted out to specialized CROs, while
for complex trials, analysis and reporting is done inhouse involving SAS
Programmers to execute the Trial Statistical Analysis Plan (TSAP). For
report writing, a medical writer is also involved.
As usual in Phase 1, standard specifications (TSAP, tables, graphs &
listings) and analysis tools (SAS macros for BA/BE/dose proportionality)
are available to handle routine tasks efficiently.
Qualification:
MSc or PhD in statistics or math. At least 2 years experience working as
a statistician in on Clinical Pharmacology studies a Pharma company /
CRO. Excellent general biostatistics knowledge. Good knowledge about
pharmacology and kinetics. Good communication skills.
2 - Consultant - 1 year contract - Task: Phase 3 trial statistician
Background information:
The candidate will work in our Clinical Biostatistics Team (11
Biostatisticians) and be responsible to support the preparation, conduct
and reporting of phase 3 trials in the respiratory area. The candidate
will work closely together with the two Project Statisticians.
Additional interfaces are to the other members of the trial teams (Trial
Manager, Data Manager and SAS Programmer) and the project teams (Project
Data Manager, the Project Statistical Programmer).
Scope of work:
The candidate will act as a fully responsible trial statistician and
will support the Project Statisticians .
In the early study conduct phase, main tasks are the definition and
review of data quality checks and the review of statistical issues
during study conduct. Thereafter, the preparation of specifications for
analysis and reporting have to be created. A prototype Trial Statistical
Analysis Plan for the entire phase 3 program of the compound has to be
written and corresponding SAS programs and outputs have to be discussed
and QC'd. Statistical standards for the projects have to be reviewed.
Depending on the scope of work the candidate may also work as a fully
responsible trial statistician for phase 2/3 trials in the diabetes
area.
Qualification:
MSc or PhD in statistics or math. At least 2 years experience working on
phase 2/3 studies in a Pharma company / CRO. Excellent general
biostatistics knowledge. Good communication skills.
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
http://www.linkedin.com/in/csmithsasstats
We will be exhibiting at the EFSPI/PSI conference at the Hilton Hotel,
Brussels on May 18th-21st. Please come and visit us on Stand 1.
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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James Miller
Department of Statistics
University of Glasgow
15 University Gardens
G12 8QQ
0141 3302474
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