Junior Statistical Programmer Analyst – Permanent Role

🔥 15 hours ago

🇨🇦 Canada – Remote

💵 $60k - $70k / year

⏰ Full Time

🟢 Junior

🖥 Software Engineer

👻 Ghost score 0%

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• Support the development and validation of datasets, tables, figures, and listings for clinical trials. • Perform programming activities using SAS and/or R under appropriate guidance and review. • Assist with processing and integrating data from internal and external sources. • Support ad hoc analyses and programming activities for clinical development and other Research & Development functions. • Assist with the development, review, and maintenance of programming specifications and documentation. • Contribute to the development and review of SDTM and ADaM datasets and specifications. • Support the preparation and review of Define-XML and other clinical trial documentation. • Work closely with Senior Statistical Programmers, Biostatisticians, Data Managers, and other cross-functional team members. • Support the programming and validation of CDISC-compliant datasets and deliverables for regulatory submissions. • Assist with the preparation of supporting documentation for electronic submissions. • Ensure programming outputs follow applicable standards, specifications, and quality requirements. • Perform programming validation and quality checks according to established procedures. • Identify, document, and resolve programming issues in collaboration with senior team members. • Ensure assigned deliverables are completed accurately and within agreed timelines. • Follow departmental programming standards, working instructions, and applicable industry guidelines. • Develop knowledge of CDISC standards, including SDTM and ADaM. • Assist in maintaining and improving programming macros, utilities, and reusable functions.

🎯 Requirements

• Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Engineering, Life Sciences, or a related discipline. • 0–2 years of experience in statistical programming, preferably within the pharmaceutical, biotechnology, CRO, or clinical research industry. • Basic to intermediate knowledge of SAS and/or R. • Familiarity with SAS programming and SAS Macro language is preferred. • Basic understanding of clinical trial data and the drug development process. • Knowledge or exposure to CDISC standards, SDTM, and ADaM is preferred. • Familiarity with clinical trial datasets, tables, figures, and listings is an advantage. • Strong attention to detail and commitment to data quality. • Ability to work effectively in a team environment and learn from senior team members. • Ability to manage assigned tasks and meet project timelines.

🏖️ Benefits

• Equal opportunity employer • Inclusive, barrier-free recruitment and selection processes • Accommodation for qualified applicants under the Human Rights Code and Accessibility for Ontarians Disabilities Act

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