Dear Allstat, 

Our client based in the South East are searching for 3 experienced contract
Statistical programmers. They are able to offer 12 month contracts with the
opportunity to be partly based from after an initial period and will wait
for 3 month notice periods. You will be assigned to mainly be working on a
major Phase II/III trial but your expertise in specific areas will be
utilised where appropriate.

If this role is of interest to you please send an updated CV to
[log in to unmask] or alternatively you can reach me on +44 (0)207
922 7126

DESCRIPTION
The Programmer will provide statistical software and software documentation
support to biometrics in general and to specific clinical projects. You will
take responsibility for the planning, development, validation, documentation
and maintenance of generic tools . Ensures that the objectives, standards,
deadlines and other requirements set by biometrics management with respect
to statistical software and its documentation and validation are attained.

GENERAL RESPONSIBILITIES

-Provides technical advice and support to biostatisticians.
-Maintains proficiency with respect to in-house computer facilities and
software.
-Interacts with members of biometrics to ensure good communication.

STANDARDS

-Develops and documents statistical programming standards in accordance with
current statistical programming practices and regulatory authority
requirements.

-Programs, validates and documents software in SAS following statistical
programming standards and ensures its availability to users. Whenever
creating new software, ensures the efficient use of existing software.


DEVELOPMENT

-Ensures that programming activities performed within the project are
executed in a timely manner and to the required high reporting standards.

-Assists in the development of trial protocols, trial analyses, editing
procedures and data presentations relating to efficacy and safety data and
evaluability under the direction of the responsible project statistician.

-Creates the datasets specification according to the global standard in
cooperation with clinical programming.

-Provides SAS datasets in the format required for special evaluations.

-Performs analyses of efficacy and safety data, generates tabulations and
graphs and provides them to members of the Biostatistics Team.

-Maintains up-to-date project documentation including that of presentation,
analysis and graphics software.


QUALIFICATIONS

-BSc, MSc or PhD (or equivalent) in Statistics, Computer Science,
Mathematics or other analytical field.
-Good knowledge of international clinical research and drug development.
-Confident in the use of Computers; can readily learn new software
applications
-Experience in programming and using statistical software as well as
knowledge of databases and interface systems. Very good knowledge of SAS.
-Able to communicate in English.
-Travel may be required


INTERPERSONAL SKILLS

-Communicates clearly and effectively in written reports, data presentations
and meetings as required.

-Establishes and maintains good working relationships; is co-operative.
Takes cultural and value differences into account in dealings with others.

-Leadership skills and an international perspective




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