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M
Associé analytique, R&D | R&D Analytical Associate
Medisca
QC
- Full-time
Relevant du/de la superviseur(e), R&D, Études et soutien technique, l’objectif principal du poste d’Associé analytique, R&D est de soutenir le développement et l’évolution des produits et…
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T
Technical Project Manager
Tesla
Markham, ON
- Full-time
PMP certification or equivalent project management training
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P&
Associate Director, Global Trade – DT/GT & Automated Export Control Systems (AECS) / Directeur associe, Commerce international – DT/GT et systemes automatises de controle des exportations (AECS)
Pratt & Whitney
Mississauga, ON
- Full-time
Agir à titre de conseiller principal en commerce international dans le cadre d’initiatives liées aux technologies de l’information et à la transformation des affaires, avec une connaissance…
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P&
Associate Director, Global Trade – DT/GT & Automated Export Control Systems (AECS) / Directeur associe, Commerce international – DT/GT et systemes automatises de controle des exportations (AECS)
Pratt & Whitney
Longueuil, QC
- Full-time
Agir à titre de conseiller principal en commerce international dans le cadre d’initiatives liées aux technologies de l’information et à la transformation des affaires, avec une connaissance…
Added 2 months ago
CR
Associate Principal/Cybersecurity & Incident Response (Forensic Services practice)
Charles River Associates
Toronto, ON
- $175,000 to $225,000 CAD / year
As an experienced leader in the forensic & cyber investigations space, your responsibilities as an Associate Principal may include (but are not limited to):
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OW
Oliver Wyman -Commercial Effectiveness and Private Capital Senior Consultant/Associate/Engagement Manager/Principal
Oliver Wyman
Toronto, ON
- Full-time
Supporting Partners in project execution through excellent project management, including work planning, workflow management, and coaching, mentoring, and formal career development support…
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I
Senior Mechanical Designer
Introba
Victoria, BC
- Full-time
…the guidance of, and per the instructions provided by, the Associate and/or Principal-in-Charge, including but not limited to performing engineering calculations, drafting, coordinating…
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P&
Gestionnaire principal, Flux de matériaux intégrés | Senior Manager, Integrated Material Flow
Pratt & Whitney
Longueuil, QC
- Full-time
Added 2 months ago
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Associate Director, Epidemiological Statistical Programming FSP
Cytel
Canada
- Full-time
…you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving…
Added 2 months ago
GI
Associate, Electrical
Global Infrastructure
Victoria, BC
- $105,200 to $120,000 CAD / year
- Full-time
The Associate forms a viable part of the Introba team and is responsible for managing their respective projects for the company. The Associate provides technical support and management…
Added 2 months ago
SG
Senior Project Architect
SJ Group
Vancouver, BC
- Full-time
Its technical experts deliver sustainable solutions that cover the entire project life cycle from planning and design, through to delivery and management, as well as a full suite of…
Added 3 months ago
C
Construction Safety Consultant position – Specialist
CrossSafety
St. Thomas, ON
- Full-time
We are currently seeking passionate and detail-oriented Construction Safety Consultants to join our team at Associate, Specialist and Principal seniority ranks. This is a salaried contract…
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Construction Safety Consultant position – Specialist
CrossSafety
London, ON
- Full-time
We are currently seeking passionate and detail-oriented Construction Safety Consultants to join our team at Associate, Specialist and Principal seniority ranks. This is a salaried contract…
Added 3 months ago
C
Construction Safety Consultant position – Associate
CrossSafety
St. Thomas, ON
- Full-time
We are currently seeking passionate and detail-oriented Construction Safety Consultants to join our team at Associate, Specialist and Principal seniority ranks. This is a salaried contract…
Added 3 months ago
C
Construction Safety Consultant position – Associate
CrossSafety
London, ON
- Full-time
We are currently seeking passionate and detail-oriented Construction Safety Consultants to join our team at Associate, Specialist and Principal seniority ranks. This is a salaried contract…
Added 3 months ago
TH
Corporate Paralegal
The HGA Group
Edmonton, AB
- Full-time
Reporting to the Principal, the Corporate Paralegal is responsible for maintaining corporate minute books, ensuring timeliness and excellence in completion of simple corporate transactions…
Added 2 months ago
MU
Research Assistant (Sustainable Management)
McGill University
Montreal, QC · Bronfman Building
- Part-time
We are seeking a motivated and detail-oriented Research Assistant to support a research project in sustainable operations management.
Added 4 months ago
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Transportation Lead, Western Canada
Entuitive
Calgary, AB
- Full-time
Responsible for effective project management including managing project budgets and schedules using appropriate project control methods and resourcing plans to meet the needs of project…
Added 3 months ago
Associate
Smith + Andersen
Kelowna, BC
The Kelowna office of Smith + Andersen is currently seeking an Associate for our Electrical team. You are a natural leader who thinks outside the box. You’re glad to collaborate with your…
Added 3 months ago
I
Associate Principal, Electrical (P.Eng)
Introba
Vancouver, BC
- Full-time
The Associate Principal is responsible for managing their respective Project Design Team. They are fully responsible and accountable for their design team staff, regularly review staffing…
Added 4 months ago
I
Senior Mechanical Designer
Introba
Toronto, Ontario
- Full-time
…the guidance of, and per the instructions provided by, the Associate and/or Principal-in-Charge, including but not limited to performing engineering calculations, drafting, coordinating…
Added 3 months ago
Associate - Electrical
Smith + Andersen
Ottawa, ON
The Ottawa office of Smith + Andersen is currently seeking an Associate for our Electrical team. You are a natural leader who thinks outside the box. You’re glad to collaborate with your…
Added 5 months ago
A
Associate Principal | Electrical Engineering
Arup
Toronto, Ontario
- Full-time
Act as Project Manager or Project Director on major multidisciplinary projects, overseeing scope, schedule, budget, resources, risk management, and overall project performance.
Added 4 months ago
GI
Senior Mechanical Designer
Global Infrastructure
Toronto, Ontario
- $86,400 to $105,000 CAD / year
- Full-time
…the guidance of, and per the instructions provided by, the Associate and/or Principal-in-Charge, including but not limited to performing engineering calculations, drafting, coordinating…
Added 2 months ago
Senior Finance Business Partner
Compeer Financial
Compeer, Alberta
Benefits: medical, dental, vision, HSA/FSA, life & AD&D insurance, short-term and long-term disability, wellness program & EAP

Cytel

Associate Director, Epidemiological Statistical Programming FSP

Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Aug 18, 2026

Original job description

Sponsor-dedicated

JOB DESCRIPTION

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Principal Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.

Position Overview

The Associate Director, Epidemiological Statistical Programming serves as a senior technical leader within the Epidemiology programming function, providing functional guidance, technical expertise, and mentorship to statistical programmers while also contributing directly to complex epidemiological projects. Working with a high degree of independence, this individual translates project and scientific objectives into effective programming strategies, proactively manages priorities and deliverables, and provides expert technical consultation to team members and cross-functional partners.

The Associate Director is responsible for leading and supporting the implementation of statistical programming activities across epidemiological and real-world evidence studies, ensuring that analyses and data outputs are accurate, reproducible, consistent, and delivered to a high standard of quality. This role may provide technical oversight of internal and external programming resources, including CRO partners, and will establish and promote programming standards, efficient processes, and best practices across projects.

In addition to hands-on project responsibilities, the Associate Director will play an important role in developing programming capabilities within the team by mentoring colleagues, reviewing and advising on technical approaches, identifying opportunities for process improvement and automation, and helping ensure appropriate allocation and execution of programming work. The individual will collaborate closely with epidemiologists, statisticians, data scientists, and other cross-functional partners to support the generation of high-quality evidence across multiple therapeutic areas.

Responsibilities

As an Associate Director, Epidemiological Statistical Programming, your responsibilities will include:

Provide technical and functional leadership to statistical programmers supporting epidemiological and real-world evidence (RWE) studies, including mentoring team members, providing technical guidance, and promoting consistent, high-quality programming practices.
Lead and contribute hands-on to statistical programming activities for epidemiological studies across multiple therapeutic areas, translating study objectives, protocols, and statistical analysis plans into robust and reproducible analytical solutions.
Develop, validate, and maintain high-quality SAS and/or R programs to support the creation of analysis datasets, statistical outputs, tables, figures, and other data products required for epidemiological research and evidence generation.
Partner closely with epidemiologists, statisticians, data scientists, and other cross-functional stakeholders to determine appropriate programming approaches and ensure analyses are implemented accurately and efficiently.
Provide expert technical consultation on complex programming, data, and analytical challenges, identifying appropriate solutions and advising team members and project stakeholders on best practices.
Oversee and review programming deliverables to ensure accuracy, reproducibility, consistency, quality, and adherence to agreed timelines and standards.
Support programming activities using a variety of real-world and observational data sources, which may include administrative claims, electronic health records, registries, and other healthcare databases.
Lead or contribute to the development of analysis-ready datasets and programming specifications, including data transformations, derivation logic, quality-control procedures, and documentation necessary to ensure transparent and reproducible analyses.
Establish, enhance, and promote programming standards, reusable tools, macros, code libraries, documentation, and quality-control processes that improve efficiency and consistency across epidemiological projects.
Drive continuous improvement and identify opportunities for automation, standardization, and innovative programming approaches that enhance the scalability and quality of epidemiological programming activities.
Contribute to the planning and prioritization of programming activities across projects, proactively identifying resource needs, technical risks, dependencies, and potential challenges to successful delivery.
Support scientific deliverables including regulatory and health authority requests, publications, abstracts, presentations, evidence-generation activities, and other analyses supporting clinical development, medical affairs, and/or value and access objectives.
Ensure programming activities are conducted in accordance with applicable regulatory requirements, company policies, SOPs, data privacy requirements, and industry best practices.
Lead or contribute to the development and maintenance of SOPs, work instructions, programming conventions, and other documentation governing epidemiological statistical programming activities.
Foster strong collaboration across internal and external teams and contribute to the development of programming talent through coaching, knowledge sharing, technical review, and mentorship.

Qualifications

Here at Cytel, we want our employees to succeed, and we enable that success through consistent training, development, and support. To be successful in this position, you will have:

Bachelor’s degree or higher in Statistics, Biostatistics, Epidemiology, Computer Science, Data Science, Mathematics, or a related quantitative discipline; advanced degree is a plus.
8+ years of relevant statistical programming experience within the pharmaceutical, biotechnology, CRO, healthcare, or life sciences industry, with demonstrated experience supporting epidemiological, observational, real-world evidence (RWE), HEOR, and/or related research.
Experience with Optum and Truveta.
Advanced programming expertise in SAS and/or R, with demonstrated ability to develop, validate, and maintain complex analytical programs and reproducible programming workflows.
Strong experience working with large and complex healthcare data sources, such as administrative claims, electronic health records (EHR), patient registries, or other real-world data sources.
Demonstrated understanding of epidemiological study designs, statistical analysis methods, and the application of programming techniques to observational and real-world research.
Proven ability to provide technical leadership and guidance to statistical programmers, including mentoring colleagues, reviewing programming approaches and deliverables, and resolving complex technical challenges.
Experience leading or coordinating programming activities across multiple projects, including prioritizing deliverables, identifying risks and dependencies, and ensuring work is completed to established quality standards and timelines.
Experience overseeing and reviewing programming deliverables.
Experience with line managing a team.
Strong commitment to programming quality, reproducibility, documentation, and the development and implementation of programming standards and best practices.
Ability to work independently, exercise sound technical judgment, and effectively manage multiple priorities in a dynamic, cross-functional environment.
Excellent written and verbal communication skills, with the ability to communicate complex technical concepts effectively to both technical and non-technical stakeholders.
Strong collaboration and leadership skills, with demonstrated ability to influence, mentor, and build effective working relationships across multidisciplinary and geographically dispersed teams.

Preferred Qualifications (Nice To Have)

Master’s degree or higher in Statistics, Biostatistics, Epidemiology, Data Science, Computer Science, or another relevant quantitative discipline.
Experience programming across multiple epidemiological and real-world data sources and/or therapeutic areas.
Experience supporting regulatory-grade RWE, regulatory submissions, health authority requests, or other evidence-generation activities.
Experience with additional programming languages, technologies, and analytical tools such as Python, SQL, Git, Unix/Linux, R Markdown/Quarto, Shiny, or similar tools.
Experience developing reusable programming tools, packages, macros, automated workflows, or other solutions that improve programming efficiency, quality, and scalability.
Experience contributing to programming standards, SOPs, work instructions, technical guidance, or organizational best practices.
Experience with cloud-based analytics platforms and/or modern data environments.

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More about this job

Responsibilities

The Associate Director provides technical leadership and mentorship to statistical programmers while executing complex epidemiological and real-world evidence studies. They are responsible for developing reproducible analytical solutions and ensuring the quality and accuracy of data outputs across multiple therapeutic areas.

Requirements

Candidates must have a bachelor's degree in a quantitative field and at least 8 years of statistical programming experience in the pharmaceutical or life sciences industry. Proficiency in SAS or R and experience working with large healthcare data sources like EHR and claims are essential.

Skills

SAS
R
Epidemiological Statistical Programming
Real-World Evidence
HEOR
Technical Leadership
Data Analysis
Clinical Development
Mentorship
Project Management
Quality Control
Regulatory Submissions
Optum
Truveta
Electronic Health Records
Administrative Claims

Visa sponsorship

Not detected in the job text

Keywords

SAS
R
Epidemiology
Real-World Evidence
RWE
HEOR
Biostatistics
Optum
Truveta
Electronic Health Records
EHR
Administrative Claims
Data Science
Clinical Development
Medical Affairs
Regulatory Submissions
Python
SQL
Git
Unix/Linux
R Markdown
Quarto
Shiny
Cloud Analytics
SOPs
Pharmaceuticals
Biotechnology
CRO
Healthcare Data
Statistical Analysis Plans

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Jobs in Canada