Principal Statistical Programmer New Remote, Canada

Precisionscientia; Canada; Remote; CAD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a skilled SAS Programmer to support and lead programming efforts for clinical trials. This role involves developing, testing, and validating SAS programs, ensuring compliance with industry standards, and providing technical expertise. The ideal candidate will have extensive experience in the Biotech or Pharmaceutical sectors, with a strong understanding of statistical analysis and project management. Join a forward-thinking company that values innovation and collaboration, where your contributions will directly impact the success of critical projects in the realm of precision medicine.

Qualifications

• 8+ years of SAS programming experience in Biotech or clinical trials.
• Strong knowledge of ICH guidelines and CDISC data structures.

Responsibilities

• Lead SAS programming efforts for clinical trials and studies.
• Generate SDTM and ADaM datasets for analysis of clinical data.

Skills

SAS Programming

Statistical Analysis

Project Management

Communication Skills

Problem Solving

Quality Control

Organizational Skills

Education

Bachelor's degree in Statistics

Bachelor's degree in Mathematics

Bachelor's degree in Computer Science

Tools

SAS

CDISC Standards

ICH Guidelines

Job description

Position Summary:
Support, lead, and provide oversight to SAS programming efforts for specific projects and studies, including developing, testing, maintaining, validating, and documenting SAS programs to meet project needs; Provide technical expertise to the development of programming standards and procedures. May serve as the project manager for assigned projects.

Essential functions of the job include but are not limited to:

• Review CRFs, edit check specifications and table mock-ups
• Create specifications for SDTM and ADaM datasets
• Oversee generation of blankcrf.pdf aCRFs and define.xml files
• Generate SDTM and ADaM datasets, tables, listings, and figures to support the analysis of clinical trials data
• Provide programming support to supplemental or exploratory analyses for regulatory agencies or any other internal and external ad-hoc requests
• Perform quality control (including documentation) for SAS programs and other study documents (e.g., presentations and reports)
• Review, maintain and approve study documents per standard procedures
• Interact with clients and lead statistical programming efforts for the project team; serve as the primary project team representative, delegating work as appropriate
• Prepare reports (i.e. patient profiles, SAP related outputs, interim analysis) for Data Monitoring Committees (DMCs)
• Assist with training of new hires; provide ongoing training and mentorship for statistical programmers
• Participate Lead or oversee in the development and maintenance of departmental procedures/standards
• Program, test and document global utility programs and tools in accordance with standards and validation procedures
• Provide technical oversight and leadership when needed for analysis and reporting; may serve as the project manager for assigned projects
• Other duties as assigned

Qualifications:

Minimum Required :
Bachelor's degree in Statistics, Mathematics, Computer Science, or in a related field; 8+ years SAS programming experience (preferably in Biotech / clinical trials / related industry)

Other Required:

• Knowledge of industry standards, such as ICH guidelines, CDISC data structures, 21 CFR Part 11 and FDA guidelines
• Broad programming experience supporting clinical trials in the Biotechnology / Pharmaceutical / CRO Industry

Preferred:

• SAS Certified Advanced Programmer for SAS 9 or equivalent proficiency
• Broad experience with Oncology and Rare Diseases
• Broad experience with ISS/ISE programming and submissions

Skills:

• Excellent organizational skills, time management, and the ability to coordinate workload to meet established deadlines
• Excellent communication and interpersonal skills to effectively interface with others (both internally and externally to foster client relationships)
• Excellent problem solving skills
• Ability to program/QC more complex analysis datasets and outputs (i.e. tables, ADaMs, efficacy related outputs, figures) in an efficient and readable manner
• Demonstrated proficiency in interpreting statistical analysis plans
• Sound judgment/decision making
• Ability to establish and teach others to maintain effective working relationships with coworkers, managers, and clients
• Service oriented, accountable and flexible
• Keen attention to detail in reviewing outputs for project deliverables
• Ability to fulfill a variety of data-related roles while building company strength and experience in data activities
• Follow and train others on applicable regulations, including FDA, ICH, and Precision Policies and Procedures

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

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