Job Description: JOB SUMMARY 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 environment. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. – Send us your resume – Vacancy of interest: Job Category: Programmer Job Type: Full Time Job Location: Hyderabad No of Openings: 5 Experience: 5 Years Job Code: CSS01A
Job Description: JOB SUMMARY 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 environment. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. – Send us your resume – Vacancy of interest: Job Category: Programmer Job Type: Full Time Job Location: Hyderabad No of Openings: 5 Experience: 5 Years Job Code: CSS01A
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.,