Penn Foster
Senior Statistical Programmer
Penn Foster, Piscataway, New Jersey, United States,
Come Join Our Growing Team!We are looking for a
Senior Programmer, Statistical Programming
to join our team in
Piscataway, New Jersey.What The Job Entails:Perform SAS data processes and analysis programming.Work with Statistician and Statistical programmer to assure results are consistent with expectations, and quality control (QC) procedures are followed.Collaborate to meet study deliverables and timelines for statistical data analysis and reporting.Plan and carefully document differences between programming results between program developer and Statistical QC programmer.Provide programming support on ISS/ISE and post-submission activities.Respond flexibly and rapidly to programming requests.Ensure consistency and adherence to standards within the project.Confirm that tracking sheets are current for projects and that results are consistent with earlier generated results.Maintain up-to-date study documentation.Develop, program, test and maintain computer validation/edit checks in SAS.Validate peer programming.Provide technical expertise and support to Data Management team. Routinely interface with cross-functional team members.Participate in regular team meetings and provide input when appropriate.Participate in the programming processes from study startup to database lock, managing project priorities and timelines.Possess good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.Requirements:BS degree or higher in programming or statistics.SAS experience in Pharmaceutical or equivalent: >=3 years. Oncology experience preferred.Good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.Strong SAS programming / Macros development / SAS graphs skills.Excellent oral and written skills for cross-site and cross-function collaboration.Dependable, motivated, focused and detail-oriented.Ability to take direction as needed and work independently on projects when necessary.Capable of managing time effectively and adhering to timelines and project schedules.Working knowledge of SAS modules and utilities.Ability to develop routines using the SAS Macro Language.Understanding of biotech industry regulatory requirements.Ability to use Microsoft Office tools: Word, Excel, PPT, etc.
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Senior Programmer, Statistical Programming
to join our team in
Piscataway, New Jersey.What The Job Entails:Perform SAS data processes and analysis programming.Work with Statistician and Statistical programmer to assure results are consistent with expectations, and quality control (QC) procedures are followed.Collaborate to meet study deliverables and timelines for statistical data analysis and reporting.Plan and carefully document differences between programming results between program developer and Statistical QC programmer.Provide programming support on ISS/ISE and post-submission activities.Respond flexibly and rapidly to programming requests.Ensure consistency and adherence to standards within the project.Confirm that tracking sheets are current for projects and that results are consistent with earlier generated results.Maintain up-to-date study documentation.Develop, program, test and maintain computer validation/edit checks in SAS.Validate peer programming.Provide technical expertise and support to Data Management team. Routinely interface with cross-functional team members.Participate in regular team meetings and provide input when appropriate.Participate in the programming processes from study startup to database lock, managing project priorities and timelines.Possess good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.Requirements:BS degree or higher in programming or statistics.SAS experience in Pharmaceutical or equivalent: >=3 years. Oncology experience preferred.Good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.Strong SAS programming / Macros development / SAS graphs skills.Excellent oral and written skills for cross-site and cross-function collaboration.Dependable, motivated, focused and detail-oriented.Ability to take direction as needed and work independently on projects when necessary.Capable of managing time effectively and adhering to timelines and project schedules.Working knowledge of SAS modules and utilities.Ability to develop routines using the SAS Macro Language.Understanding of biotech industry regulatory requirements.Ability to use Microsoft Office tools: Word, Excel, PPT, etc.
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