Statistical Programmer II

Ora; United States; Remote; USD 95,000 - 130,000; Full time

Job summary

Ora is seeking a Statistical Programmer II to support clinical trials with statistical analyses and dataset generation. You will validate SDTM datasets, develop analysis datasets, and produce tables, listings, and figures in alignment with the SAP and client requests.

Strong SAS programming skills and experience with CDISC SDTM/ADaM are essential. The role involves collaboration with senior programmers to ensure quality and timely delivery in a fast-paced environment.

Qualifications

• Degree in a scientific field or equivalent experience (not specified in ad).
• Proficient in SAS for clinical trial programming and reporting.
• Experience with SDTM/ADaM datasets and validation processes.

Responsibilities

• Provide statistical programming support for clinical trials.
• Generate/validate SDTM datasets and analysis datasets.
• Create tables, listings, and figures per SAP and client requests.
• Develop SAS macros and utilities to speed up programming tasks.
• Participate in QC activities and program validation.
• Contribute to SDTM/aCRF development and CDISC standards.

Skills

SAS

SDTM

ADaM

Macros

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