Dear Allstat:
Role: Senior Statistician - England / Scotland - Permanent
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.
Duties:
* Be familiar with and follow the departmental and company standard
operating procedures (SOPs) and
working practices (WPs).
* 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.
Strong knowledge of statistical principles underlying clinical trials, and
strong statistical skills.
SAS programming skills, familiarity of other statistical packages
Experience: A minimum of 2 years experience in statistics.
I also have a variety of other Biometric specific vacancies available in the
UK and throughout Europe.
Inclusive of SAS programming, Statistical, Data Management functions, please
call me for further details....
If you would like to discuss this role in greater detail or your application
/ suitability to this or further roles, please call me or e-mail me in
confidence. If you are not available or suited to this position, please feel
free to pass my details on.
For a confidential consultation call Mathew Hogan on 0044 (0) 207 255 6665
or email your CV to [log in to unmask]
<mailto:[log in to unmask]>
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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