Senior Statistical Programmer

Catalyst Clinical Research, LLC; Wilmington (NC); Remote; USD 80,000 - 110,000; Full time

Job summary

Join a forward-thinking company as a Senior Statistical Programmer, where your expertise in SAS programming and statistical analysis will drive innovative solutions in the biopharmaceutical industry. In this fully remote role, you'll collaborate with researchers to create analytical tools and algorithms that enhance clinical studies. With a focus on quality and data integrity, you'll play a vital role in ensuring accurate reporting and analysis. This is an exciting opportunity to contribute to groundbreaking research while working with a dynamic team dedicated to advancing healthcare solutions.

Qualifications

• Master’s degree in Computer Science, Mathematics, or related field required.
• Two years of experience as a Statistical Programmer or SAS Developer.

Responsibilities

• Develop and customize software applications for scientific projects.
• Design bioinformatics algorithms and perform data analysis.

Skills

SAS Programming

Statistical Analysis

Machine Learning

Data Validation

Bioinformatics Algorithms

Education

Master’s in Computer Science

Bachelor’s in Computer Science

Tools

SAS

CDISC Standards

Job description

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology , a full-service oncology CRO,andmulti-therapeutic global functional and CRO services through Catalyst Flex . The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com .

As a Senior Statistical Programmer you will develop new software applications or customize existing applications to meet specific scientific project needs. Create novel computational approaches and analytical tools as required by research goals. Consult with researchers to analyze problems, recommend technology-based solutions, or determine computational strategies. Keep abreast of new biochemistries, instrumentation, or software by reading scientific literature and attending professional conferences. Design and apply bioinformatics algorithms including unsupervised and supervised machine learning, dynamic programming, or graphic algorithms. Program routine and customized data displays, (including listings, tables, and graphics) in accordance with the approved Statistical Analysis Plan and shell displays. Code is to be written using SAS, SAS procedures, or standardized macros. Create safety and efficacy SAS datasets. Create project specific macros and formats. Perform data checks as needed, to ensure integrity and correctness of data displays and to understand structure and content of data. Perform QC/validation of datasets, tables, listings, figures to verify the output. Establish, maintain, and strengthen professional working relationship with clients, potential clients, regulatory agencies, collaborating staff, vendor, and subcontract personnel. Represent department and company in a multi-disciplinary setting, including project team meetings, client meetings/presentations. Ensure the quality and integrity of data analysis and reporting. Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to management. Contribute to the development of functional-level standards, tools, and templates. Interact across operational areas as required. Interact with sponsor representatives as required.

Requirements:

• Master’s* degree in Computer Science, Mathematics or related field of study.
• Two (2) years related experience as a Statistical Programmer, SAS Developer Associate or any related position requiring statistical programming as core job duty.
• Two (2) years of experience with each of the following is required: Programming Tables; Listings, and Figures; Utilizing CDISC/SDTM/ADaM and SAS programming; Developing custom SAS programs; Creating SDTM Specifications; and Handling P21 reporting and DEFINE, SDRG, and ADRG development.
• *The employer will accept a Bachelor’s degree in Computer Science, Mathematics or related field of study plus four (4) years related experience as a Statistical Programmer, SAS Developer Associate or any related position requiring statistical programming as core job duty.
• Four (4) years of experience with each of the following is required: Programming Tables, Listings, and Figures; Utilizing CDISC/SDTM/ADaM and SAS programming; Developing custom SAS programs; Creating SDTM Specifications; and Handling P21 reporting and DEFINE, SDRG, and ADRG development in lieu of a Master’s degree and 2 years’ experience.
• Up to 5% domestic travel required. 100% Remote