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Research Study Jobs in Ontario (NOW HIRING)

Mackenzie Health

Research Coordinator

Maple, ON · On-site +1

The role involves supporting study oversight, participant recruitment, data collection, and compliance with ethical and regulatory standards. In addition, the Research Coordinator facilitates study ...

Mackenzie Health

Research Coordinator

Richmond Hill, ON · On-site +1

The role involves supporting study oversight, participant recruitment, data collection, and compliance with ethical and regulatory standards. In addition, the Research Coordinator facilitates study ...

Humber River Health

Research Associate

Toronto, ON

CA$49.91 - CA$62.43/hr

Job summary: to consult on the design and execution of research studies and analysis of research data; to provide methodological expertise on research projects; to help develop an academic culture ...

Humber River Health

Research Associate

Toronto, ON

CA$49.91 - CA$62.43/hr

Job summary: to consult on the design and execution of research studies and analysis of research data; to provide methodological expertise on research projects; to help develop an academic culture ...

AFG Inc

CA$850/wk

An active email address to receive study invitations and participation details Benefits: * Take part only in studies that match your interests and schedule * Research types include online or in ...

AFG Inc

CA$850/wk

An active email address to receive study invitations and participation details Benefits: * Take part only in studies that match your interests and schedule * Research types include online or in ...

AFG Inc

CA$850/wk

An active email address to receive study invitations and participation details Benefits: * Take part only in studies that match your interests and schedule * Research types include online or in ...

AFG Inc

CA$850/wk

An active email address to receive study invitations and participation details Benefits: * Take part only in studies that match your interests and schedule * Research types include online or in ...

AFG Inc

CA$850/wk

An active email address to receive study invitations and participation details Benefits: * Take part only in studies that match your interests and schedule * Research types include online or in ...

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Research Study information

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$34

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How much do research study jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for research study in Ontario is $34.40, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $39.66 per hour, depending on experience, location, and employer.

What is a research study?

A Research Study job involves conducting investigations to gather, analyze, and interpret data on a specific topic. Professionals in this role design experiments, collect information from various sources, and summarize findings to contribute to scientific or academic knowledge. They may work in universities, healthcare, corporate research, or government agencies. Responsibilities can include literature reviews, data collection, statistical analysis, and report writing.

What are the typical daily responsibilities of someone working in a research study role?

Daily responsibilities in a Research Study role often include collecting and managing data, recruiting and coordinating with study participants, and maintaining accurate documentation of research activities. You may also be involved in designing study protocols alongside lead researchers, analyzing results using statistical software, and preparing progress reports or manuscripts for publication. Collaboration is common, as you'll work closely with principal investigators, research assistants, and sometimes external partners. Attention to detail and strict adherence to ethical standards are important in ensuring reliable and valid study outcomes.

What are the key skills and qualifications needed to thrive in the research study position?

To succeed in a Research Study position, you typically need strong analytical skills, attention to detail, and a background in scientific or social science research methodology—usually supported by a relevant degree. Familiarity with data analysis software like SPSS, R, or Python, as well as experience with survey tools and ethics certifications (such as CITI training), is frequently required. Excellent written and verbal communication, organization, and collaboration skills set top candidates apart. These competencies are crucial for accurately collecting, analyzing, and presenting data while working effectively within multidisciplinary research teams.

What kind of careers are in research study?

Careers in research study include roles such as research coordinators, data analysts, research assistants, and principal investigators. These positions often require skills in data collection, analysis, and reporting, and may involve working in clinical, academic, or industry settings with adherence to ethical standards and regulatory guidelines.

What are the most commonly searched types of Research Study jobs in Ontario?

The most popular types of Research Study jobs in Ontario are:

What are popular job titles related to Research Study jobs in Ontario?

For Research Study jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Research Study jobs in Ontario look for?

The top searched job categories for Research Study jobs in Ontario are:

Research Study jobs near you
Infographic showing various Research Study job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $71,549 per year, or $34.4 per hour.

Research Project Manager I

Hamilton, ON • On-site

Hamilton Health Sciences
See more jobs at Hamilton Health Sciencesexternal

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

The Research Project Manager I is to lead a team in the conduct of one or more research studies and accountable to the Principal Investigator (PI), (Associate) Program Manager/Program Director, Research Operations, and is responsible for the site and data management of clinical and patient based research studies, the supervision and training of study staff, and is the primary contact for internal support departments (statistics, contracts, finance, integrated technologies) and external stakeholders (sponsor, granting and funding agencies, investigational product packagers and distributers, study steering committees, and national leaders). Responsibilities include: Development and monitoring of study timelines and key deliverables in collaboration with internal and external stakeholders and project team members; With support from PI and/or operational leaders, request and evaluate various external vendors (e.g., CROs, drug depots, translation services, etc.) and facilitate contracts and budget negotiations with chosen vendors;  Provide coordination and direction in the development of data management methodologies for multiple studies; including key data management methods such as; data collection, entry, verification, data validation, quality control, adjudication tracking and event reporting for large clinical data; Evaluate and review high level study reports for compliance, safety, and central monitoring for the duration of the trial and manage communication; Develop investigator training procedures and provide investigator site training to participating centres and external stakeholders; Assist investigational site staff with the accurate and timely completion of ethics and regulatory documents in accordance with the regulatory and GCP guidelines; Supervise and train project office staff; Development of research study budgets[ Support Principal Investigator(s) in preparation of proposals, grant budgeting and writing as it pertains to human resources, investigator site payments, Investigation product (if applicable), IT and system requirements, general study administration, licensing and operations for submission to local, national, and international granting agencies and organizations; Confirm that all relevant clinical and research methodology is applied and study procedures and documents meet ICH-GCP guidelines, national and international standards and guidelines (as applicable) for good clinical practice as this pertains to accountabilities in overall research study management, site management, data management, grants and financials and staff training.; and Verify all PHRI study operations and procedures are met according to SOP's, provincial and national legislature, and practices or procedures set forth.

1. Undergraduate degree in Science or Health Science.
2. A clinical research certification (CCRP, ACRP or post-graduate certification in clinical research) is preferred.
3. Minimum of 3 years' experience in multi-centre research studies and the management of large clinical research datasets.
4. 3 years supervisory experience and team coordination experience.
5. Excellent communication, problem solving skills and ability to work flexible hours.
6. Knowledge of ICH-GCP Guidelines and international research requirements.
7. Broad knowledge of research methodology, clinical trials and drug development processes.

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