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Dear Allstat,
SEC Recruitment are currently recruiting for a few new positions recently obtained from our clients, please see below details on each of the roles:
CONTRACT: Senior Statistical Programmer
12 months renewable contract
£Negotiable
Job Summary:
Working for this major pharmaceutical client within their statistics team, you will plan & lead study / project activities for data reporting.
Accountabilities/Responsibilities:
Working on different therapeutic areas, including Oncology, within phase II-IV trials you will be required to develop expertise in the use of SAS and other in-house reporting systems and the use / set-up of
the reporting environment, programming high quality tables / listings / graphs, analysis datasets, project databases & working closely with statisticians to implement plans for trials.
Training will be given in all Client specific tools and processes.
Essential Skills & Capabilities:
·
Educated to BSc level in computing / life sciences / mathematical / statistical subject
·
4 years+ Statistical programming experience gained within the Pharmaceutical / CRO / Biotech industry
·
The ability to use / develop advanced SAS macros
·
SAS/base, SAS/macro, SAS/stat, SAS/graph
·
A good understanding of different phases / types of clinical trial reporting & the goals of reporting clinical data.
Desirable Skills & Capabilities:
Preference will be given to candidates who have therapeutic knowledge in the field of Oncology.
Ref: 217/11a
Lead Statistical Programmer / SAS Developer – SAS Drug Development
11 month rolling contract
** In depth SAS DD training will be provided for the right candidate **
START DATE: ASAP, but they will wait for the right candidate/ notice periods.
Summary:
SEC Recruitment is seeking a highly skilled SAS Statistical programmer with expert SAS development knowledge to join a major our biopharmaceutical client
on a rare and challenging freelance opportunity. The project will be on the basis of an 11 month rolling contract and lead the UK support function for SAS Drug Development (SDD)
The contract will draw on both your statistical programming skills and your experience in developing SAS tools and SAS environments.
Requirements:
With proven solid statistical programming experience gained within the pharmaceutical industry the successful candidate will be an expert SAS programmer
for clinical trials with a strong knowledge of SAS/Base, SAS/MACRO, SAS/Stat, SAS/Graph, CDISC, SDTM & ADaM. You will have experience in creating SAS Macros and SAS tools to increase operational efficiency. You will be comfortable communicating between Data
Management, IT, Statistics and Programming departments.
Experience with transfer of data across different systems, process development/improvement within a SAS programming department, system validation and standardisation
is essential.
Although the purpose of this contract has a speciality within SDD, prior use is not essential as in-depth training will be provided to become the on-site
expect. Obviously if you have experience already this will be a commodity in the application process being highly desirable.
Ref:153/11c
CONTRACT: 3 x SAS Programmer
North, UK
12 month rolling contract
Job Summary:
Working for this pharmaceutical giant you will deliver high quality SAS databases, tables, listings and graphical reports to the project team. This output is used to support regulatory submissions, publications
and commercial activities.
The job involves close project working with all members of a team particularly Statisticians for whom the programmer develops the analysis databases. The programmers also take an active part in protocol
and CRF review. They are also responsible for the specification of the tables and listings template shells and the analysis data sets. All programming work is performed to client developed GCP documentation standards.
Preferably degree or equivalent in science, mathematical or computer based subject or equivalent work experience.
Base: Particularly basic data step manipulation, SAS dataset creation, variable derivation and use of base procedures etc.
Reporting: Tabulate, Print, Report, Graph procedures
Statistics: Good skills with basic statistical summaries like Summary, Freq etc. Some skills with more formal statistical procedures such as GLM would be useful but is not essential.
Macro: Basic use of macro preferred but advanced use is not essential.
Pharmaceutical and Clinical Trials
SAS Programming
If you would like 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 further details or a confidential conversation please contact me directly: +44(0)207 2556600 or via email to
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Best regards,
Priya
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