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Section: Healthcare & Nursing Vacancy 268 |
| Post:Statistician*Programmer
|
Salary contractual |
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| Requirements and conditions |
| Age: |
Has no value
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| Gender |
Has no value
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| Education: |
no
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| Work schedule: |
Has no value
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| Work place: |
Birmingham
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| The announcement text: |
Our client is seeking contract study statisticians or programmers to join their Stats team for 6 months based in Ely, Cambs. There may be some flexibility with working from home for the right candidate.
The Study Statistician*Programmer will be a member of the clinical team and will be responsible for statistical*programming input to the reporting of clinical studies. The Study Statistician*Programmer must ensure that activities and processes performed are conducted according to company requirements.
Major Responsibilities:
* Act as a representative Statistician*Programmer on study teams, managing your time so as to provide timely input.
* SAS programming to support the Statistical reporting, including production of listing, tables and figures, for Phase II and Phase III clinical studies.
* Program*perform statistical analyses of data.
* Statisticians will be required to interpret analysis results, ensuring validity of conclusions.
* Perform quality control review of study results.
* Act as a statistical*programming contact.
* Interact with Data Management personnel as necessary to ensure that the data are in usable format; perform appropriate diagnostics prior to database locking.
* Interact with report writers in the production of integrated clinical reports and other documents containing information from clinical study databases.
* Explore data for product profiling, hypothesis generation, new research topics and publications.
* Input into the development of departmental processes, including standard working practices and operating procedures.
Qualifications and Skills:
* A relevant Batchelors or Masters degree required, with at least three years of relevant pharmaceutical experience.
* Good knowledge of applicable regulatory requirements and guidelines, e.g. ICH Guidelines.
* Proficient in the use of computers using the Windows Operating System and Microsoft Office products.
* A high level of computer proficiency, including SAS programming ability, is required.
* Good understanding of clinical data, including data quality issues
* This position holder must be able to work without close supervision
* Well-developed time management skills.
* Able to work in a fast-paced, team-oriented environment.
* Possess excellent interpersonal and communication skills (written and verbal).
* Strong attention to detail with a view to bring studies to a quality conclusion.
* Flexible, positive, creative thinker, good communicator.
Salary £Depending on skills and experience.
Please attach full and up to date CV in first instance.
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| Contact information |
| Employer: |
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| Email: |
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| Phone: |
01223 451400
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Publication date: 2009-03-26 11:46:37
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