We are currently seeking a Senior SAS Programmer Clinical Data Scientist to join our Joint Replacement Division. This is a hybrid position based onsite in Mahwah New Jersey two to three days per week.
What you will do
As the Senior SAS Programmer you will be responsible for implementation of SAS programming in support of clinical trials including: generation of data tables listings and reports using SAS; independent validation of statistical programming; assisting in the preparation of statistical analysis plans; contribution to statistical section of clinical trial protocols; generation of real-world evidence from various data sources and supporting new and ongoing clinical research initiatives. Ensure timely delivery of tables listing and summaries requested by users using SAS.
Ensure timely delivery of tables listing and summaries requested by users using SAS.
Develop SAS programs to generate clinical evidence from Real-world data sources (e.g. national registries hospital registry commercial datasets etc.)
Periodically review and report on data trends and cleanliness. Do meta-analysis of data across studies to support business needs.
Provide programming and statistical analysis support for FDA annual/final submission post marketing study reports EU MDR submission ODEP rating submissions and publication in professional journals.
Support publications by providing reports and statistical analyses to researchers and Investigators.
Interface with biostatistician as needed for complex analyses to support publications and reports.
Provide input and review statistical analysis plan (e.g. specifications of analysis data sets pooled data sets listing summaries figures and tables) for Investigational Device Exemption (IDE) clinical studies post-marketing studies and other Real-world clinical trials
Creation study reporting using RAVE reporting functions BO4 and SAS/R
Validation study summary report using SAS or R
Participate in continuous (breakthrough) improvement activity and process reengineering projects in support of Stryker Orthopaedics continuous improvement and global clinical initiatives.
What you need
Required
Bachelors Degree in a technical and/or scientific discipline
2 years of SAS programming experience with 1 years in a clinical environment
Demonstrated SAS report programming skills and be able to independently handle in-house SAS related requests
Comfortable working with AIenabled tools (e.g. AIassisted coding data exploration or documentation) and willing to adopt new analytical technologies.
Strong programming fundamentals with the ability to learn and apply additional languages tools or platforms as needed.
Demonstrated working knowledge of statistical methods and principles that are commonly used in clinical trials and be able to assist biostatistician conducting data analysis
Working knowledge of data processing database design and organization in clinical data environment
Basic knowledge of Food and Drug Administration (FDA) regulations and Standard operation procedures (SOP) as they apply to clinical studies
Preferred
Bachelors degree in Biostatistics Statistics Computer Science or related field
M.S. in health/science-related field
Industry experience in medical technology or pharma
2 years of experience in clinical data management supporting device or pharmaceutical clinical trials
Experience working with cloudbased data platforms such as Snowflake Databricks Azure or AWS
Experience with additional programming languages such as R and/or Python for statistical analysis automation or advanced analytics
Comfortable working in hybrid analytics environments combining SAS with modern tools such as R Python cloud platforms and AIenabled workflows
US20: $100000 - $166600 USD Annual
Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
Required Experience:
Senior IC
Work Flexibility: HybridWe are currently seeking a Senior SAS Programmer Clinical Data Scientist to join our Joint Replacement Division. This is a hybrid position based onsite in Mahwah New Jersey two to three days per week.What you will doAs the Senior SAS Programmer you will be responsible for imp...
Work Flexibility: Hybrid
We are currently seeking a Senior SAS Programmer Clinical Data Scientist to join our Joint Replacement Division. This is a hybrid position based onsite in Mahwah New Jersey two to three days per week.
What you will do
As the Senior SAS Programmer you will be responsible for implementation of SAS programming in support of clinical trials including: generation of data tables listings and reports using SAS; independent validation of statistical programming; assisting in the preparation of statistical analysis plans; contribution to statistical section of clinical trial protocols; generation of real-world evidence from various data sources and supporting new and ongoing clinical research initiatives. Ensure timely delivery of tables listing and summaries requested by users using SAS.
Ensure timely delivery of tables listing and summaries requested by users using SAS.
Develop SAS programs to generate clinical evidence from Real-world data sources (e.g. national registries hospital registry commercial datasets etc.)
Periodically review and report on data trends and cleanliness. Do meta-analysis of data across studies to support business needs.
Provide programming and statistical analysis support for FDA annual/final submission post marketing study reports EU MDR submission ODEP rating submissions and publication in professional journals.
Support publications by providing reports and statistical analyses to researchers and Investigators.
Interface with biostatistician as needed for complex analyses to support publications and reports.
Provide input and review statistical analysis plan (e.g. specifications of analysis data sets pooled data sets listing summaries figures and tables) for Investigational Device Exemption (IDE) clinical studies post-marketing studies and other Real-world clinical trials
Creation study reporting using RAVE reporting functions BO4 and SAS/R
Validation study summary report using SAS or R
Participate in continuous (breakthrough) improvement activity and process reengineering projects in support of Stryker Orthopaedics continuous improvement and global clinical initiatives.
What you need
Required
Bachelors Degree in a technical and/or scientific discipline
2 years of SAS programming experience with 1 years in a clinical environment
Demonstrated SAS report programming skills and be able to independently handle in-house SAS related requests
Comfortable working with AIenabled tools (e.g. AIassisted coding data exploration or documentation) and willing to adopt new analytical technologies.
Strong programming fundamentals with the ability to learn and apply additional languages tools or platforms as needed.
Demonstrated working knowledge of statistical methods and principles that are commonly used in clinical trials and be able to assist biostatistician conducting data analysis
Working knowledge of data processing database design and organization in clinical data environment
Basic knowledge of Food and Drug Administration (FDA) regulations and Standard operation procedures (SOP) as they apply to clinical studies
Preferred
Bachelors degree in Biostatistics Statistics Computer Science or related field
M.S. in health/science-related field
Industry experience in medical technology or pharma
2 years of experience in clinical data management supporting device or pharmaceutical clinical trials
Experience working with cloudbased data platforms such as Snowflake Databricks Azure or AWS
Experience with additional programming languages such as R and/or Python for statistical analysis automation or advanced analytics
Comfortable working in hybrid analytics environments combining SAS with modern tools such as R Python cloud platforms and AIenabled workflows
US20: $100000 - $166600 USD Annual
Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongsid
... View more
Job Location:
Monthly Salary:
Posted on:
Vacancies:
