Dear allstaters,


 


please find below the latest UK based Permanent Statistician role

 
 
Basic Purpose of Job:
 
To act as the lead statistician on selected single projects.  To support the
lead statistician on projects, by providing statistical input into clinical
trials from design, through analysis and reporting.  To support the lead
statistician on projects, by providing statistical input into clinical
trials from design, through analysis and reporting.  To provide statistical
programming support for data summaries and listings, and validation
programming support in the production of statistical appendices.  To
represent the Biostatistics department within the company and with
interactions with client companies and regulatory agencies, as required.
 
 

Supervisory responsibilities:          Mentoring of Associate
Statistician/Statistical Programmer (as required)

 

 

Duties and Responsibilities (according to relevant guidelines, laws and
SOP's)

 

*            Serve as a lead statistician on selected single projects.

*            Ensure projects are well documented consistent with company
SOPs and working practices.

*            Time management of own and team's time spent on projects.

*            Interact with the sponsor on statistical aspects of the
project.

*            Produce sample size calculations.  Provide input into study
design and statistical considerations, during

           protocol development.  Review protocols for completeness,
appropriateness of clinical design and sound 

           statistical analysis.  Contribute to writing appropriate protocol
sections.

*            Provide randomization schemes and appropriate documentation, on
selected projects.

*            Develop statistical analysis plans, including table, listing
and graph specifications.

*            Specify the general structure of the analysis database, provide
programming support for its development and 

          validation.

*            Produce statistical analyses and statistical appendices, with
appropriate documentation.

*            Validate statistical analyses and statistical appendices, with
appropriate documentation.

*            Prepare Statistical Reports, Integrated Summaries of Safety,
Integrated Summaries of Efficacy and other

           documents, as required.  Contribute statistical methods section
for Integrated Clinical Statistical Reports.  

           Review Integrated Clinical Statistical Reports.

 

 

 

Qualifications:  BSc degree in statistics or related field.  Advanced degree
(MSc) is desirable.

 

 

 

 

Skills and knowledge:  Strong knowledge of statistical principles underlying
clinical trials, and strong statistical skills.

                                                  SAS(r) programming skills,
familiarity of other statistical packages e.g. StatXact, Nquery) and
understanding of database structures.

                                                  Familiarity with ICH
Statistical and reporting guidelines and GCP.

                                                               

 

 

Experience: A minimum of 1 years experience in statistics in a clinical
research environment.

 

 
 
If this role is of interest please contact me for further details. 
 
Or please forward this onto relevant persons who my find this role of
interest.
 
 
Mathew Hogan
Senior Consultant
Pharmaceutical, Biometrics & CRO Division

1st Pharma People
A Division of 1st-IT People
Tel: +44 (0) 207 255 6665
Fax: +44 (0) 207 255 6656
 <mailto:[log in to unmask]>
mailto:[log in to unmask]
 <http://www.1st-pharmapeople.com/> www.1st-pharmapeople.com
 
PLEASE NOTE: As of 31st May 2005 our office address will change to; 1st IT
People, 3rd Floor, Woolverstone House, 61-62 Berners Street, London. W1T
3NJ. As a result of this, we do have a new telephone number of 0207 255
6665. Please note our previous phone number will still work.
 
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This email is confidential and intended solely for the use of the 
individual to whom it is addressed. Any views or opinions presented are 
solely those of the author and do not represent those of the company from 
which the email was sent. If you are not the intended recipient, be advised 
that you have received this e-mail in error and that any use, dissemination 
forwarding, printing or copying of this e-mail is strictly prohibited. 
While every effort has been made to scan this e-mail, we can not accept any 
responsibility for loss of business or damage caused arising from this
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