Principal Statistical Programmer

Jobtailor; Warren; On-site; CAD 70,000 - 90,000; Full time

Job summary

Jobtailor in Canada seeks an experienced SAS programmer to support clinical trial analysis and reporting. You will work within multidisciplinary teams to ensure data quality, comply with regulatory standards, and deliver analysis datasets, TFLs, and reports in line with project strategies.

Responsibilities include adhering to programming standards, guiding analyses, and partnering with study teams to meet regulatory timelines.

Qualifications

• Masters degree required in a relevant field.
• 3+ years of SAS programming experience.
• Experience with clinical trial data and reporting.

Responsibilities

• Provide timely support to the study team on programming matters according to project strategies.
• Assist in implementing programming and project standards.
• Support and/or lead programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements.
• Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval.

Skills

SAS Programming

Clinical Trial Analysis

Data QC

Education

Masters Degree

Tools

SAS Base

SAS Stat

SAS Macro

SAS Graph

Programming Standards

Data Analysis

Data Reporting

QC of Analysis Datasets

TFLs

User Requirements

Job description

• Provide timely support to the study team on all programming matters according to the project strategies
• Assist in providing guidance in implementing and executing the programming and project standards
• Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements
• Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval

Requirements

• Masters Degree
• SAS (Base, Stat, Macro, graph)
• 3+ Years experience

Core Competencies

Demonstrates expertise in SAS programming, including Base, Stat, Macro, and Graph, to support clinical trial analysis and reporting. Collaborates effectively within multidisciplinary teams to ensure adherence to project standards and regulatory requirements.

Highest-signal resume keywords

• SAS Programming
• Clinical Trial Analysis
• Data Quality Control
• Regulatory Compliance
• Masters Degree

ATS Optimization Keywords

Hard Skills

• SAS Base
• SAS Stat
• SAS Macro
• SAS Graph
• Programming Standards
• Data Analysis
• Data Reporting
• QC of Analysis Datasets
• TFLs
• User Requirements

Industry Keywords

• Clinical Trials
• Regulatory Approval
• Multidisciplinary Team
• Project Strategies
• Data Models