Statistical Programmer: Junior and Senior

at  Valos

REQUIRED QUALIFICATION AND EXPERIENCE

• University degree (or equivalent) in mathematics, statistics, informatics or related disciplines.
• Good knowledge of programming languages and of data management principles and tools.
• Experience in SAS programming within a pharmaceutical company

Or

• Experience working within a clinical research organization

Or

• Experience in programming including working within a pharmaceutical company or a clinical research organization.
• Ability to communicate effectively in English.

• Responsible of implementation and use of programs able to effectively analyze and report clinical trial data.
• Supports the implementation of computerized systems/tools that can facilitate the trials/projects data analysis, handling and flow, including the handling of organizational aspects.
• Responsible of the definition of project and trial analysis databases. Informs and suggests solutions to the statistician on critical issues within the project.
• Performs the programming for trial or project specific data reports and statistical evaluations in agreement with the guidelines of the statistician and/or the project statistical programmer, as appropriate, aimed to guarantee quality deliverables according to contractual obligations and ICH-GCP guidelines.
• Discusses data presentation methods with the appropriate members of the project team.
• Informs and suggests solutions to the biostatistics head on critical programming issues within the project.
• Performs the programming for standard and special analyses and provides the appropriate members of the project team with trial or project specific listings, summary tabulations and graphics.
• Maintains up-to-date documentation for the reporting, analysis and graphics software that is under his responsibility.
• Provides technical advice and support to other project team members.
• Assesses, recommends and develops new standards, policies and procedures.
• Supports computerized systems/subsystems implementation that facilitate the handling and the documentation of trial specific or project specific CRF or non-CRF data, including data flow monitoring and reporting tools, according to the project quality requirements.
• In agreement with the statistician and/or project statistical programmer, designs and implements trial and project analysis database structures and programs the algorithms that are to be applied to the data for the conversion between different database structures.