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Added 9 mins ago
Customer Service Associate
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Quebec, QC · Galeries de la Capitale
…career that’s suited to them, whether that’s at our stores, head office, or Campus in Quebec City. Proud to recognize our teams’ contributions, we provide competitive work conditions as…
Added 22 mins ago
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- $17.95 CAD / hour
- Full-time
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PhD Scholarship in China Studies at the Department of Cross-Cultural and Regional Studies, Faculty of Humanities, University of Copenhagen (UCPH)
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AstraZeneca

Quantitative Pharmacoepidemiologist

Mississauga, ON, Canada
Canada - Mississauga, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 1, 2026
Posting language: English
Posted: Oct 8, 2026

Original job description

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe.

Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office and in downtown Toronto are purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.

Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.

AstraZeneca’s Safety Epidemiology team is a global group of PhD-trained pharmacoepidemiologists with expertise in conducting epidemiological studies, performing evidence synthesis and analytics to evaluate drug safety. The team plans and delivers R&D safety epidemiology activities that inform the benefit–risk profiles of nearly 100 marketed and pipeline products. These activities include local and global post-authorisation regulatory commitment studies (PARCS) submitted to health authorities such as the FDA and EMA.

Safety Epidemiology offers a dynamic, inclusive and supportive environment where epidemiologists can build rewarding careers and make meaningful contributions to drug development, pharmacoepidemiology and public health. We welcome applications from recent PhD graduates and postdoctoral researchers in epidemiology who are interested in drug safety, real-world data analysis and a career in the pharmaceutical industry.

The quantitative pharmacoepidemiologist role will report to the Senior Director, Safety Epidemiology and is a pivotal scientific role within Global Patient Safety, accountable for performing rapid analyses of large electronic healthcare databases from around the world to support PARCS planning, signal detection, predictive clinical safety, clinical trial planning, drug development, new drug applications to regulatory authorities and to support responses to health authorities (e.g., FDA , EMA etc).

The incumbent will be responsible for delivering high-quality descriptive epidemiological analyses of real-world healthcare data across various products in the AZ portfolio. The role applies analytical methods to generate robust evidence from electronic healthcare databases and collaborates with multidisciplinary teams to address scientific and business questions. Key responsibilities include programmatic specification of a research question, analytical study execution, data interpretation, programming, evidence generation, and communication of findings to internal collaborators across Global Patient Safety, Global Regulatory, Global Medical/Clinical functions.

Essential Requirements

Ph.D. in pharmacoepidemiology, epidemiology, public health, biostatistics or related health science field and substantial hands-on experience analysing large electronic healthcare data (relational databases) and other real world data sources (claims, registry or other secondary healthcare databases)
Advanced level skills in syntax-based SAS or R
A strong interest in pursuing a career in pharmacoepidemiology and drug safety
Able to apply epidemiological theory and techniques to solve new and challenging problems
Conceptual understanding of real-world data for secondary research use, and the data generation mechanism that impact how such data is analysed
Ability to translate a research question into an implementable query that can be run in a real-world database
A strong interest in data management and using data to improve health within the pharmaceutical industry
Able to work effectively with internal & external collaborators, including collaborative groups and contract research organizations (CROs)

Desirable Requirements

PhD dissertation in pharmacoepidemiology or epidemiology with a strong focus on medicines as the exposure of interest
Ability to work independently to achieve specific research objectives
Hands-on experience planning, analysing and interpreting results of statistical analyses performed using large electronic healthcare data or other real-world data
An approach passionate about using imperfect data and finding practical ways to move forward in addressing research objectives
Ability to prioritize and work pragmatically to generate results rapidly to support health authority requests and/or insights needed to further clinical development
Working knowledge of epidemiological methods used in research in drug development or in a closely related academic research area

Are you interested in working at AZ, apply today!

AstraZeneca is committed to taking every reasonable precaution to protect employees, our customers and the healthcare systems in the communities in which we serve. In an effort to protect the wellbeing of our employees and customers, full COVID-19 vaccination is an essential requirement of all positions at AstraZeneca. As such, all offers of employment will be conditional upon either (i) proof of full COVID-19 vaccination or (ii) proof of need for accommodation under relevant human rights legislation, and AstraZeneca’s determination that the requested accommodation can be provided without undue hardship. You will be required to submit proof of full vaccination or proof of need for accommodation during our background screening process.

AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com.

We are using AI as part of the recruitment process.

This advertisement relates to a current vacancy.

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More about this job

Responsibilities

The incumbent will perform rapid analyses of large electronic healthcare databases to support drug safety, regulatory submissions, and clinical development. They are responsible for delivering high-quality descriptive epidemiological analyses and collaborating with multidisciplinary teams to address scientific questions.

Requirements

Candidates must hold a Ph.D. in pharmacoepidemiology, epidemiology, public health, biostatistics, or a related field. Substantial hands-on experience analyzing large electronic healthcare data and advanced proficiency in SAS or R are required.

Skills

Pharmacoepidemiology
Epidemiology
SAS
R
Drug safety
Real-world data analysis
Statistical analysis
Data management
Evidence synthesis
Regulatory submissions
Clinical trial planning
Signal detection
Electronic healthcare databases
Public health
Biostatistics

Benefits

Collaborative culture
Flexible working arrangements
Professional development

Visa sponsorship

Not detected in the job text

Keywords

Pharmacoepidemiology
Epidemiology
Drug safety
Real-world data
SAS
R
Electronic healthcare databases
Regulatory affairs
FDA
EMA
Biostatistics
Public health
Clinical development
Signal detection
Evidence synthesis
Data management
PARCS
Pharmaceutical industry
Predictive clinical safety
Claims data
Registry data
Statistical programming
Research methodology
Multidisciplinary collaboration

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