Clinical Research Coordinator
2 weeks ago
**Clinical Research Coordinator / Psychometrist, Sunnybrook Research Institute**
(Temporary Full-time, one year term with option to renew)
**Location**:
Sunnybrook Health Science Centre Research Unit
(2075 Bayview Avenue, Toronto, Ontario)
**Reports to**:
Dr. Sandra Black
**Hours**:
Typical 37.5 hour work week, with some flexibility based on patient schedules, and the ability to work after hours as needed
**DESCRIPTION**
**KEY RESPONSIBILITIES**
- Interact with elderly volunteers and patients with dementia, movement disorders and/or stroke
- Conduct and score neuropsychological tests, including computerized testing and caregiver questionnaires for ongoing pharma clinical trials and observational studies
- Administer a variety experimental, neurocognitive and clinical measures, including gait and eye-tracking assessments
- Maintain research databases which include patient demographics, clinical, neuropsychological, neuroimaging and genetic variables etc.
- Organize blood sample collection and assist with data entry
- Function as part of a patient-focused team of professionals
- Maintain ongoing, professional communication with staff (doctors, fellows, residents and co-workers) in order to help maintain comprehensive patient care
- Triage patient phone calls as well as calls from families, and other departments with diplomacy and courtesy, ensuring the appropriate personnel are notified of the phone message
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
Please be advised that to be eligible for employment at Sunnybrook, all new hires must have received the full series of a COVID-19 vaccine or combination of COVID-19 vaccines approved by Health Canada (e.g., two doses of a two-dose vaccine series, or one dose of a single-dose vaccine series); AND have received the final dose of the COVID-19 vaccine at least 14 days ago. Medical exemptions or any other kind of requested exemption based upon the Hospital’s obligations pursuant to the Ontario Human Rights Code will be considered on a case-by-case basis.
Sunnybrook Research Institute is committed to providing accessible employment practices that are 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.
Please be advised that in order to be eligible for employment at Sunnybrook, all new hires must have received the full series of a COVID-19 vaccine or combination of COVID-19 vaccines approved by Health Canada (e.g., two doses of a two-dose vaccine series, or one dose of a single-dose vaccine series); **AND** have received the final dose of the COVID-19 vaccine at least 14 days ago. Medical exemptions or any other kind of requested exemption based upon the Hospital’s obligations pursuant to the Ontario Human Rights Code will be considered on a case-by-case basis.
-
Clinical Research Coordinator
2 weeks ago
Toronto, Canada Headlands Research Full timeOverview: **The Role** Toronto Memory Program is looking for a Clinical Research Coordinator to manage clinical research protocols. This individual will work directly with the investigators, and other research staff to ensure protocol visits are being conducted according to ICH GCP guidelines. **This Clinical Research Coordinator role will be based in...
-
Clinical Research Coordinator Ii
2 days ago
Toronto, Canada Centricity Research Full time**Clinical Research Coordinator II (CRC II)** **Join Us at Centricity Research!** Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient;...
-
Clinical Research Coordinator
2 weeks ago
Toronto, Canada Think Research Full time. ***ON-SITE ROLE** **The Company** BioPharma Services Inc. is a subsidiary of Think Research. BioPharma Services was founded by two surgeons dedicated to advancing medical science to improve the life and spirit of their patients. With this same dedication and vision in mind, these physicians brought life to BioPharma. Through each success, and even...
-
Clinical Trial Associate
4 weeks ago
Toronto, Canada ICON Clinical Research Full timeClinical Trial Associate - Clinical Supplies ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Supplies Clinical...
-
Research Coordinator
1 week ago
Toronto, Canada CHEO RESEARCH INSTITUTE Full time**JOB DESCRIPTION** **Posting # - RI-25-029** **Posting Period - May 30 to June 13, 2025** **POSITION: Clinical Research Coordinator** 360 Concussion Care Clinic, Toronto location New Position **TERM**: Full time, 1.0 FTE 1 year contract, with possibility of renewal **SALARY**:Commensurate with skills and experience **REPORTS TO**: Manager,...
-
Clinical Research Coordinator I
2 weeks ago
Toronto, Canada Ontario Institute for Cancer Research Full time**Position: Clinical Research Coordinator I** **Location: MaRS Centre, Toronto** **Department: OHCRN** **Reports To: OHCRN Program Manager** **Salary: Commensurate with level of experience** **Hours: 35 hours/week** **Job Type: Hybrid** **Status: Full-time, Permanent** The Ontario Institute for Cancer Research (OICR) is seeking an experienced professional...
-
Remote Clinical Trial Supplies Coordinator
4 weeks ago
Toronto, Canada ICON Clinical Research Full timeA leading clinical research organization is seeking a Clinical Trial Associate focused on managing clinical supplies. The role supports the execution of clinical trials through ordering, handling, and tracking supplies while collaborating with cross-functional teams. Candidates should have relevant qualifications, extensive experience in clinical support,...
-
Clinical Screening Coordinator
2 weeks ago
Toronto, Canada Centricity Research Full timeAventiv Research, IACT Health, LMC Manna Research, and True North Clinical Research have united to become the largest network of fully-owned and integrated clinical research sites in North America, Centricity Research. The sites that were formerly known as Aventiv operate in Ohio and Arizona and specialize in phase 1 pharmaceutical, device, and diagnostic...
-
Remote Global Clinical Project Lead
2 weeks ago
Toronto, Canada Everest Clinical Research Services Inc. Full timeA leading clinical research organization is seeking a Project Manager to oversee clinical trials and manage project teams. The role involves ensuring project milestones are met, coordinating with sponsors, and leading cross-functional teams. Ideal candidates will have extensive experience in clinical research, strong leadership skills, and fluency in...
-
Clinical Research Coordinator
2 days ago
Toronto, Canada TheOfficeChair Full timeWe are conducting the Screening rounds and an assessment sessions on behalf of our Clients for the Clinical Research coordinator roles. If qualified, your roles and responsibilities would be as follows: **Duties**: - Coordinate and oversee clinical research studies from start to finish - Ensure compliance with study protocols, regulations, and ethical...