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Biomedical Project Manager Jobs in Vaughan, ON (NOW HIRING)

... into biomedical terms and prepare statistical data results for inclusion in reports and research ... Work with data management team to ensure data captured incorporates and corresponds to project ...

... biomedical data sharing, discovery, and analysis. We build cutting-edge software and industry ... Improve how bioinformatics projects are prioritized, scoped, tracked, and documented to promote ...

... biomedical data sharing, discovery, and analysis. We build cutting-edge software and industry ... Improve how bioinformatics projects are prioritized, scoped, tracked, and documented to promote ...

... biomedical data sharing, discovery, and analysis. We build cutting-edge software and industry ... Improve how bioinformatics projects are prioritized, scoped, tracked, and documented to promote ...

Showing results 21-35

Biomedical Project Manager information

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What is a biomedical project manager?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

How does a biomedical project manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What are the key skills and qualifications needed to thrive as a biomedical project manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.
What job categories do people searching Biomedical Project Manager jobs in Vaughan, ON look for? The top searched job categories for Biomedical Project Manager jobs in Vaughan, ON are:
Infographic showing various Biomedical Project Manager job openings in Vaughan, ON as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Remote job distribution.

Research Associate, Health Technology Evaluation

University Health Network

Toronto, ON

Full-time

Posted 18 days ago


Job description

Company Description

UHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care. UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto.

UHN’s vision is to build A Healthier World and it’s only because of the talented and dedicated people who work here that we are continually bringing that vision closer to reality.

www.uhn.ca

Job Description

Union: Non-union
Number of vacancies: 1
New or Replacement Position: New
Site: Toronto Rehabilitation Institute, University Centre
Department: Research
Reports to: Senior Scientist
Salary Range: $37.85 - $47.31 per hour
Hours: 37.5 hours per week
Status: Temporary Full-Time
Closing Date: August 10, 2026

Job Summary

As an integral member of the research team, the RESEARCH ASSOCIATE I works with the study Principle Investigators, and other research team members to ensure the successful completion of designated studies, the responsibilities include: coordinating research study activities and staff/resources to meet established research goals; planning, implementing and coordinating all aspects of the research study data collection, including conducting semi-structured interview administration, data input and analysis and report production; providing functional supervision for research assistant; participating in planning of subsequent projects and with the preparation of grant proposals and papers, as appropriate; performing mid level data analysis, interpretation of results, preparation of materials for review and incorporation into reports, presentations and grant submissions; summarizing data and education of multidisciplinary staff.

Duties

  • Plan and execute technology evaluation studies using validated frameworks such as the Technology Acceptance Model (TAM) and related implementation science models.  
  • Design and conduct qualitative research, including semi-structured interviews, focus groups, and ethnographic observation, with residents, families, front-line staff, and administrators.  
  • Support quantitative data collection activities including survey administration, basic descriptive and inferential analyses, and mixed-methods integration.  
  • Apply human factors and user experience principles to evaluate the usability and safety of health technologies in LTC workflows.  
  • Design, develop, and maintain surveys and data collection instruments in REDCap, including using branching logic, validated scales, and longitudinal tracking forms.  
  • Create and maintain data dictionaries, codebooks, and standard operating procedures for data collection and management.  
  • Ensure data quality, integrity, and security in compliance with institutional and regulatory standards.  
  • Prepare and manage Research Ethics Board (REB) applications, amendments, and continuing review submissions.  
  • Ensure all research activities adhere to the Tri-Council Policy Statement (TCPS-2), applicable privacy legislation (PHIPA, PIPEDA), and institutional policies.  
  • Support informed consent processes and participant engagement, including with cognitively vulnerable populations.  
  • Facilitate co-design and engagement sessions with LTC stakeholders, including residents, substitute decision-makers, care staff, and administrators.  
  • Support the preparation of research summaries, presentations, reports, and manuscripts for peer-reviewed publication and knowledge dissemination.  
  • Contribute to grant reporting, progress reports, and funding renewals.  
  • Coordinate timelines, deliverables, and milestones across multiple concurrent research projects.  
  • Track project progress and flag risks or delays to the PI; maintain project management documentation.  
  • Liaise with external collaborators, clinical sites, technology vendors, and community partners   
Qualifications
  • Master's degree in a relevant field such as Health Services Research, Health Informatics, or Health Technology, Human Factors Engineering or Human-Computer Interaction (HCI), Occupational Therapy, Nursing, Social Work, or Allied Health (with a research or implementation science focus), Psychology, Sociology, or Public Health (with qualitative/digital health specialization), or an equivalent combination of a bachelor's degree in a related field plus substantial relevant experience may be considered.  
  • Minimum 2 years of experience conducting qualitative health research (interviews, focus groups, thematic/framework analysis).  
  • Demonstrated experience building surveys and data collection tools in REDCap.  
  • Hands-on experience with health technology platforms.  
  • Familiarity with technology evaluation and implementation science frameworks.  
  • Experience with project coordination or management in a research setting.  
  • Experience conducting research in long-term care would be an asset  
  • Strong qualitative data analysis skills; basic quantitative skills: descriptive statistics, survey analysis (SPSS, R, or similar).  
  • Understanding of human factors and/or UX research methods   
  • Excellent written and verbal communication skills, including the ability to write for diverse audiences (academic, clinical, public).  
  • Strong organizational skills with the ability to manage multiple projects simultaneously.  
  • Ability to work both independently and collaboratively in a team environment.  
  • Sensitivity and professionalism when working with older adults, persons living with dementia, and their caregivers.  

Additional Information

Why join UHN?
In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN.

  • Competitive offer packages
  • Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.com/)
  • Close access to Transit and UHN shuttle service
  • A flexible work environment
  • Opportunities for development and promotions within a large organization
  • Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.)

Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration.

All applications must be submitted before the posting close date.
UHN uses email to communicate with selected candidates.  Please ensure you check your email regularly. At University Health Network (UHN), artificial intelligence technologies may be used to assist in the screening, assessment, and selection of candidates for this position.
Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application.
UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known.
We thank all applicants for their interest, however, only those selected for further consideration will be contacted.