CLINICAL PROGRAMMER

As a Statistical Programmer I, you will be responsible for creating, testing, and maintaining programs for clinical studies using SAS. Your key responsibilities will include: - Using SAS to generate summary tables, data listings, graphs and derived datasets as per statistical analysis plan and programming specifications. - Ensuring that outputs meet quality standards and project requirements. - Performing validation programming and collaborating with team members to resolve discrepancies. - Keeping project team members informed of programming progress and issues. - Following SOPs and relevant regulatory guidelines. - Maintaining well-organized project documentation and verification/quality control documents. - Managing scheduling and adapting to timeline changes. - Contributing ideas and respecting opinions of others in internal meetings. - Willingness to collaborate with others and assist with projects as necessary. - Completing project programming activities within the given timeframe. Qualification Requirements: - Undergraduate Degree, preferably in a scientific or statistical discipline; or equivalent combination of education and demonstrated programming experience. - Proficiency in SAS programming, preferably in a clinical trial environment. - Excellent written and verbal communication skills. - Ability to read, write, speak, and understand English. No additional details of the company were provided in the job description.,