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Dear Allstat,

Senor SAS Programmer
Permanent
Based in Belgium (100% on site)
Excellent salary

A rapidly growing global biopharmaceutical company has a permanent opportunity for a Senior SAS Programmer. This is to be based in Belgium.

KEY RESPONSIBILITIES:

Supports projects through the creation and maintenance of analysis data sets, integration of safety and efficacy data, production/validation of output, and review of annotated case report forms.

Collaborates with project/study Biostatisticians and Statistical Programming Managers in the creation, implementation, and maintenance of programming development plans for each project/study accounting for timelines, resources, and quality deliverables for all project/study assigned; ensure that all programming has been carried out per appropriate validation program standards; along with appropriate documentation within the programs

- Must have experience integrating data sets from archived and current studies
- Must have experience managing programming activities and collaborating with other functions
- Experience in developing project plans including time and resource estimates
- Experience in development and implementation of statistical programming standards is preferred
- Knowledge of software systems development is a plus
- Experience using industry standards for data set design as defined by Clinical Data Interchange Standards Consortium (CDISC)
- Knowledge of appropriate FDA and other regulatory (i.e., ICH) guidance's
- Excellent working knowledge of Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH a plus. Experience using SAS version 8.2, 9.1.3 or 9.2
- Proficient in developing own code as well as modifying existing code
- Experience producing detailed and accurate documentation for statistical programs
- Excellent analytical, problem solving and organization skills with the ability to work on multiple tasks
- Flexible to changing priorities, detail-oriented, works well under pressure with initiative to take on unfamiliar tasks
- Excellent communication skills (verbal and written) as well as good interpersonal skills
- Strong organizational skills and the ability to work in a collaborative environment, and desire to improve skills are essential
- Experience working with Cru's and other Service Providers

Education & Experience Requirements:


- Bachelor's degree in a scientific field required, Master of Science degree preferred
- At least 5 years of statistical programming experience using SAS in the pharmaceutical, contract research organization, or other clinical research setting
- A SAS Certified Advanced Programmer degree or equivalent (SAS/Base, SAS/Advanced, SAS/Macro, SAS/SQL, SAS/Graph and SAS/Effective programming)
- Looking for someone with the ability to work independently and oversee deadlines with a high degree of flexibility and commitment
- Must speak Dutch

For a confidential consultation call Laura Christie on +44 207 633 4825 or email your CV to [log in to unmask]<mailto:[log in to unmask]>

I look forward to hearing from you.

Kind regards,

Laura


Laura Christie
Principal Consultant, Biometrics, Europe
Recruiting experts in Pharma

HAYS Recruiting experts worldwide
25-27 Wootton Street
London
SE1 8TG

T:  +44 207 633 4825
M: +44 7900 932031
F: +44 207 922 7101
E: [log in to unmask]<mailto:[log in to unmask]>

hayspharma.com
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