Statistical Programmer II New Remote - US

Ora Inc.; Northern (KY); Remote; USD 75,000 - 110,000; Full time

Job summary

Ora Inc. seeks a Statistical Programmer II to support clinical trials, producing analyses and SDTM datasets, analysis datasets, tables, listings, and figures. You will work under the guidance of senior programmers and contribute to the SAP review and data analysis methods.

The role emphasizes SAS programming expertise and collaboration, with duties including developing macros, ensuring quality, and validating CDISC SDTM/ADaM specifications.

Qualifications

• Experience programming for clinical trials using SAS.
• Familiarity with SDTM/ADaM standards.
• Strong statistical data analysis skills.
• Ability to work under supervision and in teams.

Responsibilities

• Perform assigned statistical programming for clinical trial analysis.
• Work under the direction of senior statistical programmers.
• Review the Statistical Analysis Plan for programming analyses.
• Apply appropriate statistical methods for data analysis.
• Assist in designing/developing SAS macros and other utilities to expedite SAS programming activities.
• Generate tables, listings, and figures per protocol, SAP, and client requests.
• Participate in statistical program validation and quality control activities.
• Assist in development of SDTM aCRF and specifications; complete programming and validation of CDISC SDTM and ADaM

Skills

SAS programming

Clinical trial data analysis

SDTM/ADaM knowledge

Statistical methods

Team collaboration

Tools

SAS

Job description

POSITION TITLE:Statistical Programmer II

Ora Values the Daily Practice of …

Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor

At Ora, we are building the future of ophthalmic clinical research. As the world’s leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past 45 years, our expert teams have helped earn more than 85 new product approvals. Ora's pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven across thousands of global projects.Today, our team continues to expand across the globe, with over 400 employees across North America, Europe, Asia, and Latin America.

The Role:

Provide statistical programming support to clinical trials. Produce statistical analyses, including generating/validating SDTM datasets, analysis datasets, tables, listings, and figures for clinical trials.

What You’ll Do:

• Perform assigned statistical programming required for clinical trial analysis and reporting .
• Work under the direction of senior statistical programmers in completing clinical trial programming tasks .
• Review the Statistical Analysis Plan in preparation for programming analyses .
• Apply appropriate statistical methods for data analysis .
• Assist in designing/developing SAS macros and other utilities to expedite SAS programming activities .
• Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request .
• Participate in statistical program validation and quality control activities, as assigned .
• Assist in development of SDTM aCRF and specifications; complete programming and validation of CDISC SDTM and ADaM