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CONTRACT: SAS Programmer - Mainland Europe
6-12 months renewable contract


Job Summary:

Working for this major pharmaceutical client, you will create;
*       Programs and output for data management and biostatistics for validation of data, for non statistical contributions of integrated study reports and for other programming requests
*       Data sets for statistical analysis


Accountabilities/Responsibilities:

Planning & deadlines
*       internal and external procedures and regulations e.g. ClinSOP's, ICH-GCP, internal standards (variable names, templates etc)
Provide data output that correctly and accurately reflects data in database according to reporting plan
*       Make planning for programming activities
*       Transform request in program code
*       Validate program code
Develop validated standard programs for general use
*       Create plan for development, implementation and testing
*       Transform requirements into program code
*       Validate programs according to validation plan
Create standard structures for databases
*       Create data dictionaries for studies according to global and project standards
*       Exchange data with other international locations
 Provide SAS data sets for statistical analysis and reports
*       Create derived data
*       Check and document the data sets provided
Develop customized programs for single use and provide solutions for ad-hoc requests
*       Transform request in program code
*       Check the program code


 Essential Skills & Capabilities:

Educated to degree level
3 years relevant work experience as a SAS Programmer
A good understanding of database structures & SAS programming
Good knowledge of standards for clinical studies (ICH-GCP)
Numerical and analytical skills
Team Player
Fluent in English (oral & writing)


Desirable Skills & Capabilities:

Preference will be given to candidates who meet the following criteria:
Knowledge and experience of SAS/Graph
CDISC
An excellent opportunity awaits for this renewable contract. Interview times booked and full job specification to review...


If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

We also have a broad variety of other Biometric specific vacancies available in the UK and throughout Europe. Inclusive of SAS programming, Statistical, Clinical programming, Data Management functions, Regulatory Affairs, Clinical Research, QA, Compliance & Validation.

For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV [log in to unmask]


James Carrera

Pharmaceutical, Healthcare & CRO Division
Tel: +44 (0) 207 255 6665         [log in to unmask]
Fax: +44 (0) 207 255 6656        www.1st-pharmapeople.com

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