Senior Biostatistical Programmers, Contract (Brussels, Belgium)
CK Clinical are pleased to announce the following positions with an global pharmaceutical company:
NATURE & SCOPE - Provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase II & III clinical trials, ISS & ISE, primarily using SAS.
- Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic submissions.
- Based on site in Brussels you will work with biostatisticians and programmers based in other sites (US-UK). Homeworking is NOT available for this position.
- This position will require a significant training investment for the use of our client 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.
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- At least 3-5 years 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.
STARTING DATE & DURATION
Starting date: October 15th (at the latest)
Contract duration: 6 months
Helena Newman-Mitchell
Biometrics Director
CK Clinical Ltd
9 High Street
Stevenage
Hertfordshire
SG1 3BG
hnewmanmitchell@ckclinical.co.uk
www.ckclinical.co.uk
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