Statisticien Programmer

Sas programmeur

Main Tasks and Responsibilities
• Providing programming support for clinical
• Generate analysis datasets according to CDISC standard
• Develop standard SAS macros for efficient analyses of clinical data
• Oversee and/or develop programs/macros/procedures used to produce statistical results of clinical data
• Creating SAS programs to generate / validate datasets, tables, figures and listings as per the study specifications and support ad-hoc requests if required
• Providing statistical input to CRF, SAP and analysis of tables, figures and listings TFLs (shells)
• Performing any other related activities assigned by the supervisor, such as the documentation of deliverables
• Maintaining all the required documentation for assigned projects and adhering to Internal SOPs and BGs
• Ensuring deliverables or outputs meet quality standards and project requirements
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• Develop and maintain relations with customers within the project responsibilities
• Business travels according the project needs.
Position Information
• Open ended contract (CDI)
• Competitive salary and the opportunity to join an international company with continued growth and strong market presence in three continents (Europe, North Africa and United States)
• On-going training
• Friendly working environment within a company that supports and develops associates of all levels. A place to definitely grow your career and reach your full potential

SAS Programmer(m/f) SAS Programmer
Type: Full time position ( télétravail)
Location:tunis, Tunisia
Reporting level: Head of Biostatistics and Programming

Job Requirements:
• Master’s degree in Mathematical, Statistical, Computer Science or Life Sciences
•  experience in Clinical SAS programming is a must
• Experience in creating SAS programs to generate / validate datasets, tables, figures and listings
• Experience in SDTM/TLF/ADAMS is preferable but not mandatory
• Fluency in English, both verbal and written
• Good communication and problem resolution skills
• Ability prioritize and balance concurrent tasks and responsibilities
• Strong project management skills

Position description
As a member of the biostatistics team,responsible for processing clinical data required for statistical analysis of clinical trials, prepare different analysis datasets as well as study reports and dashboards. This person must have ability to anticipate and understand the needs of internal and external customers and rapidly respond on their requirements.

If you are open to new challenges, ready to join a multinational team who are rapidly expanding and determined to thrive in a fast-paced environment.
(CV and cover letter, in English or French)