Research Coordinator II Research Options Lab

Unity Health; Toronto; On-site; CAD 60,000 - 75,000; Full time

Job summary

Unity Health is seeking a dynamic Research Coordinator II for the Options Collaboratory at St. Michael's Hospital in Toronto. The successful candidate will coordinate important studies focusing on HIV and STI prevention, adhering to compliance and safety protocols while engaging with diverse communities.

Qualifications

• Undergraduate Degree + 3 years relevant experience, or equivalent.
• Knowledge of healthcare terminology and research ethics.
• Strong communication skills and understanding of systemic health issues.

Responsibilities

• Coordinate study activities, manage timelines and resources.
• Assist with ethics submissions, participant recruitment, and data collection.
• Oversee research activities, budgets, and logistics.

Skills

Communication

Interpersonal Skills

Project Management

Education

Undergraduate Degree

Job description

Research Coordinator II Research Options Lab

Join to apply for the Research Coordinator II role at St. Michael's Hospital.

The Options Collaboratory (www.optionslab.ca) is seeking a dynamic team player with clinical trial experience for a Research Coordinator II position. Our interdisciplinary research team focuses on HIV and STI prevention and treatment, housed within the MAP Centre for Urban Health Solutions (www.maphealth.ca) and conducting research at St. Michael's Hospital.

The successful candidate will coordinate studies related to HIV, STIs, and emerging infectious diseases, including ethics submissions, participant recruitment, sample collection, and study documentation in compliance with regulations. Familiarity with community-engaged research and working with diverse populations, including marginalized groups, is essential.

This onsite position offers occasional remote work. We encourage applications from underrepresented communities, even if you don't meet every qualification.

Duties & Responsibilities

• Coordinate study activities, manage timelines, resources, and deliverables.
• Assist with ethics submissions, study documentation, participant recruitment, and data collection.
• Manage research compliance, safety protocols, and regulatory submissions.
• Support proposal development, grant applications, and data analysis.
• Prepare reports, publications, and presentations.
• Oversee research activities, budgets, and logistics.
• Supervise research staff, assist with hiring, onboarding, and training.

Qualifications

• Undergraduate Degree + 3 years relevant experience, or equivalent.
• Experience in clinical research; GCP, Health Canada Division 5, and TCPS CORE 2 certifications required (to be completed within 2 weeks of hire).
• Knowledge of healthcare terminology, research ethics, and project management.
• Strong communication, computer, and interpersonal skills.
• Experience working with diverse communities and understanding systemic health issues.

We value authentic cover letters that reflect your unique experiences. Accommodation requests are handled confidentially per AODA and Ontario Human Rights standards.