Dear Allstat,
My client is one of the large pharma companies, and are looking for Statisitical Programmer Co-ordinators for both London and Belgium, the contract is initially for 6 months with possibilities of Extension. They are looking for candidates to start in July. The rate is negotiable but will be around 70-75 Euros. If interested please email me an up to date CV at [log in to unmask]
DUTIES
* Provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase I - phase III clinical trials, ISS & ISE, primarily using SAS (Primarily Phase 1 at least in the beginning).
* Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic submissions.
* will work with biostatisticians and programmers based also in other sites (UK/US/BEL/GER). Homeworking is excluded for this position.
* This position will require a significant training investment for the use of conventions in SAS macros, creation of analysis data sets and dataset structures.
* Apply knowledge of clinical data, the design and phases of clinical trials, statistics, relevant regulations and the pharmaceutical industry to the implementation of tasks.
* Handle complex statistical programming issues independently and be familiar with study programming issues. Bring ideas for new projects and take the initiative to solve issues.
* Mentor and coordinate statistical programming activities for a therapeutic area worldwide.
* Provide input into trial planning documents, and perform the planning for the statistical programming activities within the given therapeutic area.
SPECIFIC SKILLS
* SAS expert
* Good written and oral communication skills in English (Fluent). Strong organizational skills.
* Ability to evaluate processes and situations in an orderly and rational manner asking questions and identifying missing information.
* Must be able to determine relationships between different parts of a problem and identify appropriate solutions.
* Strong people skills and the tact and discretion required for negotiation within a team setting to obtain cooperation and approval from other team members. Must be able to effectively interpret and explain complex information.
* Accurately and efficiently work towards quality results
EXPERIENCE
* Statistical SAS programming experience within Pharmaceutical industry.
* Working knowledge of clinical legislation (FDA, EMEA, ...), Good Clinical Practice (GCP) and Clinical Data Interchange Standards Consortium (CDISC) is a plus.
Kien-Sen Lee
Resourcer ~ Biostatistics Division
James Harvard Pharmaceutical Ltd
T. 020 7922 7126 F. 020 7922 7101
E: [log in to unmask]
W: www.jamesharvardpharma.com
25 - 27 Wootton Street : Waterloo : London : SE1 8TG
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