CONTRACT: SAS Programmer / Developer
Process Improvement Specialist
Mainland Europe
6-12 month rolling contract
Job Summary:
We are looking for a self-starting IT professional with a proven track
record of process improvement / software development. The successful
candidate will need to be comfortable in taking part in a variety of
software development / process improvement activities.
Accountabilities/Responsibilities:
The Biostatistics Infrastructure team provides functional support and
direction to the wider Biostatistics organization. For example the group:
Provides support and leadership in the implementation of CDISC SDTM 3.1.x
standards.
* Provides support and leadership in the implementation of CDISC SDTM
3.1.x standards.
* Has developed and deployed a bespoke ETL solution to manage and
automate the creation of SAS datasets that conform to CDISC SDTM data
standards (or any other data standards for that matter)
Provides ongoing development and support for a library of standard reporting
macros to implement standard table shells across study teams
* Is the main point of contact for Clinical Development Biostatistics
and the broader IS organization. This interface involves activities such as
evaluation and deployment of new SAS versions and technologies (such as
Integration Technologies, BI Server etc), the deployment of new Unix servers
to support the expanding computational needs of the department, the creation
and deployment of a Biostatistics standard pc image, support for remote
workers etc.
The group has also recently expanded its remit to include the provision of
training services to support the Clinical Development Biostatical
Programming function.
Essential Skills & Capabilities:
The candidate should be able to demonstrate an ability and willingness to
quickly acquire new IT skills. Ideally we are looking for a candidate with
the following experience:
* An in-depth knowledge of the SAS system
* Strong analysis and design skills
* Leading and managing contract resource
* An understanding of Clinical Trials within
Pharmaceutical/Biotechnology/Public Health setting in Industry, Government
or Academia
* Drug Development (Pre-clinical Development, Clinical Development,
Medical Affairs)
* Project Planning and Management
* Development of policies and SOPs
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 to [log in to unmask]
James Carrera
European Contracts Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Mobile: +44 7717 578 246
Fax: +44 (0) 207 255 6656
mailto:[log in to unmask]
www.1st-pharmapeople.com
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