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Research Study Assistant Jobs in Hamilton, ON (NOW HIRING)

Uottawa

Research Assistant

Ottawa, ON

CA$31.89 - CA$50.25/hr

  • PTO

The Research Assistant will support the scholarly activities of the Centre for International Policy Studies (CIPS). Responsibilities include taking analytical notes during conferences and seminars ...

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All JobsResearch Study JobsResearch Study Assistant JobsResearch Study Assistant Jobs in Hamilton, ON

Research Study Assistant information

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How much do research study assistant jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for research study assistant in Hamilton, ON is $23.61, according to ZipRecruiter salary data. Most workers in this role earn between $13.55 and $27.81 per hour, depending on experience, location, and employer.

How much does a research study assistant get paid?

Research study assistants typically earn between $12 and $20 per hour, depending on experience, location, and the complexity of the research. Some positions may offer additional benefits or stipends, especially in academic or clinical settings.

Is it hard to get a job as a research study assistant?

Securing a position as a research study assistant typically requires relevant education, such as a bachelor's degree in a related field, and sometimes prior experience or familiarity with research tools like data analysis software. Competition can vary depending on the institution and location, but strong organizational skills and attention to detail are often valued by employers.

What are the key skills and qualifications needed to thrive as a research study assistant?

To thrive as a Research Study Assistant, you need a solid understanding of research methods, data collection, and basic statistical analysis, often supported by a bachelor's degree in a relevant field. Familiarity with data management software (such as REDCap or SPSS) and compliance with research ethics certifications are typical requirements. Attention to detail, strong organizational abilities, and effective communication skills are vital soft skills for this role. These competencies ensure accurate data handling, adherence to protocols, and successful collaboration with research teams.

What is the difference between Research Study Assistant vs Research Coordinator?

AspectResearch Study AssistantResearch Coordinator
CredentialsTypically requires a bachelor's degree in a related fieldOften requires a bachelor's degree; some roles prefer or require additional certifications
Work EnvironmentAssists with data collection, participant recruitment, and administrative tasks in research settingsOversees study protocols, manages staff, and ensures compliance in research projects
Employer & IndustryHospitals, universities, research institutesHospitals, research organizations, academic institutions

The main difference is that Research Study Assistants support data collection and administrative tasks, while Research Coordinators manage study operations and oversee research projects. Both roles are essential in research settings but differ in responsibilities and level of oversight.

What is a research study assistant?

Research Study Assistants are professionals who support the design, implementation, and management of research studies, often in academic, medical, or scientific settings. Their responsibilities typically include recruiting participants, collecting and organizing data, maintaining study records, and ensuring compliance with research protocols. They work closely with principal investigators and other research staff to ensure studies run smoothly and efficiently. Research Study Assistants play a crucial role in maintaining data integrity and supporting the overall success of research projects.

What are some typical challenges research study assistants face when coordinating participant recruitment and data collection?

Research Study Assistants often encounter challenges such as recruiting enough qualified participants within tight timelines and maintaining participant engagement throughout the study. Managing scheduling conflicts, ensuring informed consent, and adhering to strict data collection protocols are also common hurdles. Successful assistants are proactive in communication, detail-oriented, and adept at troubleshooting unexpected issues that may arise during recruitment or data gathering. Building rapport with participants and collaborating closely with the research team helps address these challenges effectively.

What cities near Hamilton, ON are hiring for Research Study Assistant jobs?

Cities near Hamilton, ON with the most Research Study Assistant job openings:

Research Study Assistant jobs near you
Infographic showing various Research Study Assistant job openings in Hamilton, ON as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 20% Part Time, 1% Temporary, and 3% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $49,105 per year, or $23.6 per hour.

Research Project Manager I

Hamilton Health Sciences

Hamilton, ON

Full-time

Posted 2 days ago

New

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; ย 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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