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Snr Associate/Analyst,Stats Programming

CSL Code: 4435

Job Title
Snr Associate/Analyst,Stats Programming
Salary
£30,000 - £45,999
Job Type
Programming, Statistics
Location
Central/City
Employment Type
Permanent Job
Employer Type
PM Pharmaceutical R&D HQ (Global Or EU)
Seniority
Executive/Officer
Duration
 
FTE Hours
Full Time 35 - 40hrs Per Wk
Vacancy Status
Open For Applications
Date Posted
Mon 14th July 2008, 03:05pm
Are you an experienced Statistical programmer seeking a role within a leading Global Pharma?

Our client are a Japanese Global Pharma who is committed to developing and delivering healthcare products that truly benefit humanity and responds to the^diverse healthcare needs of people around the world. Our client works globally on three main therapeutic areas: CNS, Gastro-Intestinal and Oncology. They are now looking to recruit a Senior Associate/Analyst in Statistical Programming to join their^team on a permanent basis based in West London with a view to relocating to Hertfordshire early next year.

The purpose of this role would be to support the Biostatistics team by providing statistical programming and validation support for analysis datasets, statistical tables, figures, listings, patient profiles, SAS transport files, Integrated Summaries of Safety (ISS), electronic submissions, relates clinical trials and for other internal and external requests (e.g. publications).
Working with external vendors in order to develop or monitor the content and structure of SAS datasets, when necessary. Accessing and converting data to SAS from ClinTrial Database management system and PC file formats.

Qualifications and Skills required:

Bachelor's degree in associated functional discipline and MSc (biostatistics, statistics or computer science).
Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office.
Proven experience with Unix and Windows operating systems.
Understanding of the software development life cycle.
Experience in SAS programming for phase I-IV clinical trials in a pharmaceutical or CRO setting
Understanding of FDA guidelines.
Good organisation, time management and attention to detailskills

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