This position functions as a member of the Biostatistics and Statistical Programming project team supporting the Lead Statistical Programmer in the development of programs to support the conduct statistical analysis and reporting of projects. A Statistical Programmer I creates, tests and maintains programs for clinical studies, under the direction of more senior programmers. He or she participates in the creation and maintenance of Statistical Programming project documentation.
JOB RESPONSIBILITIES
Uses SAS to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications.
Works to ensure that outputs meet quality standards and project requirements.
Performs validation programming and works with other Statistical Programmers, Biostatisticians, and other project team members to resolve discrepancies or any findings.
Keeps project team members informed of programming progress and issues requiring their attention.
Follows applicable SOPs and relevant regulatory guidelines (e.g. ICH).
Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs, ensuring inspection readiness.
Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, and adapts to timeline or priority changes by reorganizing daily workload.
Prepares in advance for internal meetings, contributes ideas, and demonstrates respect for opinions of others.
Displays willingness to work with others and assist with projects and initiatives as necessary to meet the needs of the business.
Completes project programming activities within timeframe allotted by Lead Statistical Programmer and/or management.
Performs other work-related duties as assigned.
Minimal travel may be required.
QUALIFICATION REQUIREMENTS
Undergraduate Degree, preferably in a scientific or statistical discipline; In lieu of degree, an equivalent combination of education and demonstrated programming experience.
Proficiency in programming in SAS preferably in a clinical trial setting.
Excellent written and verbal communication skills.
Ability to read, write, speak, and understand English.