Jobs in Canada

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Added 2 hours ago
JI
Business Analyst | Analyste d'affaires – POS, Omnichannel & Mobile
Jesta I.S.
Montreal, QC
- Full-time
Evaluate proposed workflows from both the store associate and end-customer perspectives, with a focus on usability and operational efficiency.
Added 2 hours ago
AR
desktop support analyst
Atlas-Apex Roofing Inc.
Toronto, ON · Etobicoke, ON
- Full-time
Consult user guides, technical manuals and other documents to research and implement solutions
Added 5 hours ago
R|
Fellowship and Bursary Administrative Assistant
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the…
Added 5 hours ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the…
Added 5 hours ago
R|
Fellowship and Bursary Administrative Assistant
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the…
Added 5 hours ago
CW
Business Development Specialist, full-time position
City Wide Facility Solutions
Vancouver, BC
- $43,000 to $55,000 CAD / year
- Full-time
Find and research businesses that would benefit from City Wide's services
Added 5 hours ago
CW
Business Development Specialist, full-time position
City Wide Facility Solutions
Burnaby, BC
- $43,000 to $55,000 CAD / year
- Full-time
Find and research businesses that would benefit from City Wide's services
Added 7 hours ago
J
Senior Clinical Trial Manager (Sr CTM), Dermatology & Rheumatology
Jobgether
Canada
- Full-time
…planning through completion. Working closely with Clinical Research Associates (CRAs), sponsors, investigative sites, and cross-functional teams, you will help maintain study timelines and…
Added 8 hours ago
UO
Senior Software Developer
University of Victoria
Victoria, BC
- Full-time
The Senior Developer reports to the Associate Director, Software Development with work assigned on a project basis. This position leads scrum meetings, documentation and code reviews using…
Added 8 hours ago
SG
Associate Director, North America Regulated Utilities, Infrastructure Ratings
S&P Global
Toronto, ON
- Full-time
…of North America's most critical infrastructure assets. As Associate Director, the role carries responsibility for leading end-to-end credit analysis across an assigned portfolio of North…
Added 9 hours ago
Associate Advisor, People, AMI
FortisBC
Surrey, BC
Coordinate and maintain AMI People information within SharePoint and assist in research.
Added 10 hours ago
TU
Research Associate
The University of British Columbia
Kelowna, BC
- Full-time
…(UBC), Okanagan campus invites applications for a full-time, Research Associate in the area of DNA nanotechnology with an anticipated start date of May 1, 2027 or a date to be mutually…
Added 10 hours ago
CU
Graduate Awards, Finance and Planning Officer
Carleton University
Ottawa, ON
- Other
The incumbent must possess the following qualifications: · In addition, the incumbent must have a dedication to the highest level of client service and high expectation for quality
Added 10 hours ago
CO
Part-Time Customer Service Associate
City of Brampton
Brampton, ON
- Part-time
- Temporary
Added 10 hours ago
OH
Regulatory Affairs Associate
Organika Health Products
Vancouver, BC
- Full-time
We are looking for a detail-oriented and proactive Regulatory Affairs Associate to join our growing team in Vancouver.
Added 10 hours ago
WA
Associate Director, Content & Community
We Are Social
Toronto, ON
- $95,000 to $115,000 CAD / year
- Full-time
We are looking for an Associate Director, Content & Community to join our growing Creative Strategy team. This is a team of curious, culturally connected thinkers with a passion for social,…
Added 10 hours ago
UO
Manager, Research and Analytic Services
University of Calgary
Calgary, AB
- Full-time
Reporting to the Associate Director (Methods and Analytics), the Manager, Research and Analytic Services leads an integrated multidisciplinary team of professional, research and technical…
Added 10 hours ago
BI
Senior Actuarial Associate, Pension Risk Transfer (PRT)
BMO Insurance
Toronto, ON
- Full-time
Participate in strategic initiatives, process improvements, and industry research.
Added 10 hours ago
WA
Associate Director, Content & Community
We Are Social
Remote, Canada
- $95,000 to $115,000 CAD / year
- Remote
We are looking for an Associate Director, Content & Community to join our growing Creative Strategy team. This is a team of curious, culturally connected thinkers with a passion for social,…
Added 11 hours ago
UO
Coordinator, OIPH Learning Health System
University of Calgary
Calgary, AB
- Full-time
The O' Brien Institute for Public Health (OIPH) is a research institute within the Cumming School of Medicine at the University of Calgary. OIPH brings together members from across…
Added 11 hours ago
LB
Associate, Investment Services
Letko, Brosseau & Associates
Toronto, ON
- Full-time
…customer base. We believe our business-minded, fundamental research approach, strong ethical culture and client-first fiduciary commitment has been the key to our long-term growth and…
Added 11 hours ago
SS
Marchés Privés - Comptabilité et administration des fonds, associé/e principal/e/Privates Markets- Fund Accounting & Administration, Senior Associate , Senior Associate
State Street
Montreal, QC
- Full-time
Privates Markets- Fund Accounting & Administration, Senior Associate
Added 11 hours ago
SS
Marché Privés - Comptabilité et administration des fonds, Officer/Private Markets- Fund Accounting & Administration, Officer
State Street
Montreal, QC
- Full-time
Added 11 hours ago
H
Clinical Research Site Supervisor
HealthCareersInSask.ca
Regina, SK
- Full-time
The Clinical Research Site Supervisor is actively involved in supporting quality assurance and quality improvement activities in the department, which would include; monitoring compliance…
Added 11 hours ago
B
Senior Actuarial Associate, Pension Risk Transfer (PRT)
BMO
Toronto, ON · YNG
- Full-time
Participate in strategic initiatives, process improvements, and industry research.

Brunel

Evidence Delivery Associate/Manager, Medical Evidence Canada

Mississauga, ON, Canada

Full-time

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Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Nov 26, 2026
Posting language: English
Posted: Oct 27, 2026

Original job description

Introduction

The Medical Evidence team at AstraZeneca Canada is comprised of Evidence Delivery and Evidence Generation. This team is responsible for leading the local management of AstraZeneca (AZ) sponsored real-world evidence (RWE) and externally sponsored research (ESR) studies. The Evidence Delivery function within the Medical Evidence Canada Team is responsible for the strategic and efficient delivery of ESR studies. The Evidence Delivery Manager, Medical Evidence will lead the delivery and oversight of ESR studies in the assigned therapeutic area. Assigned studies may span multiple therapeutic areas in the Oncology Business Unit (OBU) and Biopharmaceuticals Business Unit (BBU).

Reporting to the Director, Medical Evidence in Canada, the incumbent will work closely with the other Evidence Delivery Managers and in a cross-functional environment. Internal stakeholders include but not limited to Medical Affairs (e.g., Medical Advisor), Drug Supply, Regulatory, Patient Safety, Legal, Finance, and ESR Governance and Operations. This role involves collaboration with these teams to ensure adherence to all relevant policies and processes (e.g., AZ Standard Operating Procedures [SOPs]) to deliver studies that meet time, cost, and quality objectives. This person will also serve as the main liaison between AZ and Principal Investigators and their study teams (e.g., academic and research organizations).

Responsibilities

Support the initial triage checklist and proposal cross-functional review by evaluating the operational feasibility (e.g., availability of funds and drug supply)
Following study approval, serve as the main point of contact between AZ Global, AZ local, and the Institution (including but not limited to the Principal Investigator and study team)
Coordinate the initial protocol review and subsequent protocol amendments with the relevant stakeholders
Set up and maintain the study in Veeva Clinical Vault (e.g., upload files, enter information into fields, performance assessments)
Distribution of IBs to Investigators for interventional trials
Input regular updates into the internal study Excel trackers and support with monthly set up
Lead the drafting and executing of confidentiality disclosure agreements, supporting administrative finalization of legal documents (e.g., accepting track changes, deleting comments), and consulting with Legal as needed
Supporting the drafting and execution of research agreements and amendments
Fill out forms to retrieve key information including LoA and WBS requests
Support with adverse event reconciliation may include consultation with Patient Safety
Obtain and/or complete necessary documentation for drug supply and submit order documents (e.g., drug order forms, supply plan)
Schedule and facilitate meetings - take minutes for meetings where transcript is not used
Submit invoices, enter information into the ABACUS accounting system, update internal budget tracker, and communicate any budget issues/changes with the relevant stakeholders (e.g., Finance Business Partner, Senior Marketing Manager)
Submit publications for review using the iEnvision system and provide any follow up information requested by the Publication Coordinators

Requirements

Bachelor’s in science degree at a minimum but Master’s or doctorate level preferred
Experience in project management and/or clinical study management (e.g., operations and study design of clinical trials, drug development process in Canada, and relevant research guidelines [e.g., GCP/ICH])
Demonstrated success in building rapport and navigating cross-functional matrixed environments by leveraging strong communication to influence or align stakeholders and foster collaboration, and advance initiatives through the organization
Experience working alongside busy clinician scientists, asset if experience serving as a liaison of a pharmaceutical company
Self-motivated and able to display autonomy and initiative; for instance, able to make decisions/ move actions forward without continual supervision or consultation
Effective time management, prioritization, and organization and attention to detail to manage a dynamic and fast-paced changing environment

What We Offer

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.

About Us

Brunel has a reputation for working with some of the best in the business. That’s what we continually strive for. Over 45 years, we’ve created a global network of interesting clients and talented individuals working together through a vast array of services.

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More about this job

Responsibilities

Lead the operational delivery and oversight of externally sponsored research studies, coordinating between AstraZeneca teams, investigators, and research institutions. Manage study protocols, documentation, systems, drug supply, budgets, meetings, safety-related coordination, and publication review while ensuring compliance with applicable policies and processes.

Requirements

A bachelor's degree in science is required at minimum, with a master's or doctorate preferred, along with experience in project or clinical study management and knowledge of clinical trial operations, drug development in Canada, and GCP/ICH guidelines. The role also requires strong cross-functional communication, stakeholder collaboration, autonomy, organization, prioritization, and attention to detail.

Skills

Project Management
Clinical Study Management
Clinical Trial Operations
Study Design
Drug Development
Good Clinical Practice
ICH Guidelines
Cross-Functional Collaboration
Stakeholder Management
Communication
Protocol Review
Study Budget Management
Contract Administration
Veeva Clinical Vault
ABACUS Accounting System
Time Management

Benefits

Interview Coordination
Offer Assistance
Onboarding Assistance

Visa sponsorship

Not detected in the job text

Keywords

Externally Sponsored Research
Real-World Evidence
Clinical Study Management
Clinical Trial Operations
Study Design
Drug Development
Good Clinical Practice
ICH Guidelines
Protocol Review
Protocol Amendments
Veeva Clinical Vault
Principal Investigators
Research Agreements
Confidentiality Disclosure Agreements
Drug Supply
Adverse Event Reconciliation
Patient Safety
Study Budgeting
ABACUS Accounting System
iEnvision
Publication Review
Cross-Functional Collaboration
Stakeholder Management
Medical Affairs
Regulatory Compliance
Oncology
Biopharmaceuticals

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Work requirements

Jobs in Canada