(UA-673) | Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-11901

(UA-673) | Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-11901

01 Feb
|
Sunnybrook Health Sciences Centre
|
Ontario

01 Feb

Sunnybrook Health Sciences Centre

Ontario

Regular Full time (37.5 hours per week, Mon-Fri)
The DAN Women and Babies Program at Sunnybrook Research Institute is seeking a Research Coordinator for a full-time position to support the program and one research study. This role would provide an excellent opportunity for a recent graduate with an interest in maternal and neonatal research to further their research experiences.

1. DAN Women and Babies Program
Reporting to the Senior Research Project Manager, Susan O’Rinn, the incumbent will support research and administrative aspects of multiple projects in the area of maternal and neonatal research. Responsibilities may include:

Administrative
Provide general program administrative support including preparing meeting agendas,



taking minutes, meeting and event catering, etc.
Facilitate access (i.e. to electronic health record systems) for staff/students
Provide summer student program support for (orientation, training, award applications, etc.)
Maintain internal and external websites and various internal reports/lists
Liaise with various departmental and hospital staff as needed
Other duties as assigned

Research
Conduct literature reviews
Medical chart review & data abstraction
Assist with preparation and management of study documents and other research files including questionnaires, consent forms, and participant materials
Assist with participant recruitment and informed consent activities
Assist with the collection, management, and analysis of qualitative and quantitative data
Assist with preparation and submission of written materials such as: research ethics board applications, grant submissions, legal agreements, manuscripts, research reports, poster and presentation submissions
Coordinate data flow both internally as well as externally i.e.



with collaborators from other sites
Liaise with external personnel i.e. collaborators, sponsors, etc.
Apply general research principles, concepts and techniques to all research tasks

2. Single Dose of Antenatal Corticosteroids (SNACS) Randomized Controlled
Trial for Pregnancies at Risk of Preterm Delivery
Reporting to the Principal Investigator, Dr. Nir Melamed, this position is primarily responsible for the coordination of SNACS, a Health Canada-regulated clinical trial, but may also include some support for other studies.

Responsibilities
Participant recruitment at Sunnybrook Health Sciences Centre (ongoing screening and eligibility review of patients).




Coordination and tracking of all participants including maintaining screening and enrolment logs as well as scheduling and completing participant study visits within protocol-specified time frame.
Liaise with investigators and other study staff to ensure consistency and quality of all study procedures.
Collect, organize, manage and enter data into paper and electronic case report forms.
Prepare Research Ethics Board (REB) communication including submission of protocol amendments, annual renewals, reporting of serious adverse events and protocol deviations.
Assist with REB applications and other regulatory submissions as needed.
Communication with study monitors and participation in monitoring visits.
Maintenance of essential regulatory documents for ongoing trials.
Perform other duties as assigned.

Qualifications
Required
Bachelor’s degree in a relevant field (e.g. health research methodology, health sciences related discipline)
1-3 years of experience working in a research setting




Experience with in-person participant/patient recruitment
Familiarity with research processes including data collection and data entry
Exceptional organizational skills and attention to detail
Excellent interpersonal and communication (oral and written) skills
Ability to work both independently and collaboratively within a team environment with staff at all levels within the organization
Tact, discretion and ability to manage confidential and sensitive data and information

Preferred
Previous experience with Health Canada-regulated clinical trials
Completed training for Good Clinical Practice (GCP) quality standards, Health Canada Division 5 regulations and Transportation of Dangerous Goods regulations
Experience working in a healthcare setting
Familiarity with Research Ethics Board submissions
Excellent computer skills,



including proficiency with Microsoft Office (Excel, Word, PowerPoint)

Salary will be commensurate with experience. To apply, please send your resume to [email protected] .

Please note that by applying for this role, you are able to work on-site at Sunnybrook Health Sciences Centre

We thank all candidates for their interest but only candidates selected for an interview will be contacted. Applications will be accepted until the position is filled.

The Sunnybrook Research Institute is committed to providing accessible employment practices in compliance with the Accessibility for Ontarians with Disabilities Act (‘AODA’). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.





Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ persons, and all others who may contribute to the further diversification of ideas.

The original job offer can be found in Kit Job:
https://www.kitjob.ca/job/90600639/ua-673-research-coordinator-sri-evaluative-clinical-sciences-regular-full-time-2025-11901-ontario/?utm_source=html

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