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Job Details:
 
Information about the position
Job Number:    6112
Job Title:    Senior Statistical Programmer
Date Posted:    1/8/2010

Job Description:    JOB ROLE: The Senior Statistical Programmer is responsible for all programming aspects (analysis datasets, pooled datasets, listings and tables) of individual Phase I-IV clinical trials and project level activities for small drug project/indications. PRINCIPAL RESPONSIBILITIES include: • To lead the programming activities for a trial, early phase project, indication, or publication activities • Maintain efficient interfaces with internal and external customers with support of the Project Leader and the Program Statistician. • Develop resource plans as required • Develop and comply with project / study standards and specifications following internal guidelines. • Make certain that documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures tables, listings and figures for phase I-IV clinical trials and submission activities. • Program, according to specifications, analysis datasets, pooled datasets, listings, tables, and figures for phase I-IV clinical trials and for SCS and SCE with high quality and within milestones. • Maintain records for all assigned projects and archiving of trial / project analysis and associated documentation. • Participate in the selection of CROs and supervise the SR trial activities of the CROs.

Platform:   

Required Skills:    QUALIFICATIONS, KNOWLEDGE & EXPERIENCE: • BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field. • Significant experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry • Intermediate knowledge of / experience with SAS software. • Working knowledge of database design/structures

Desired Skills:    PERSONAL SKILLS & ATTRIBUTES: • Fluent in English both oral and written • Good office tool skills • Good understanding of global clinical trial practices, procedures, methodologies. • Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH)

Duration:   
Start Date:   
Location:    South East England
Travel:   
Rate:   

Information about the company
Company Name:    Fforde Management Ltd
Contact Person:    Chris Brown
Contact E-Mail Address:         chris@fforde-management.com
Company Web Site:         www.fforde-management.com
Phone Number #1:    01273 722967
Phone Number #2:    01273 222967
Fax Number:   

Job Poster's Comments:    Our client, a global giant in the pharmaceutical world, is known as a leading name in the discovery, development and marketing of innovative pharmaceutical products which cure diseases, ease suffering and enhance the quality of life. They are seeking a Senior Statistical Programmer for their offices in the South East UK.



 

 

 

 

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