Clinical SAS Programmer

• Provide quality deliverables by following corporate and departmental policies, procedures and applicable standards.
• Perform data manipulation, analysis and reporting of clinical trial data.
• Create analysis files, tables, listings, and figures and validation of those files.
• Maintain project tracking and validation documentation.
• Work well in an environment where team members may be distributed across multiple locations.
• Review planning documents (Statistical Analysis Plan, dataset specifications, etc.) to ensure project objective alignment, clarity, accuracy and completeness of programming requirements.
• Present statistical programming concepts to non-programming team members as necessary.
• Collaborate effectively with cross-functional teams and interface with multiple stakeholders to manage timelines and priorities.
• Serve as back-up to Principle Statistical Programmer as needed.

Requirements:

• BA/BSc in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject with at least 8 years of relevant experience or Master's degree and at least 5 years.
• Prior regulatory submission and response experience.
• Excellent analysis and reporting skills.
• Command of drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.
• Knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards.
• Ability to work effectively and successfully in a dispersed team environment with cross-cultural partners.
• Excellent oral and written English communication skills.
• Excellent time management skills, able to meet required timelines.
• Ability to provide quality output and deliverables, in adherence with timelines.
• Willingness and ability to learn and follow standard processes and procedures.