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Research Coordinator
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Research Coordinator
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Research Coordinator
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University of Toronto Toronto, CanadaDate Posted: 04/23/2024 · Req ID: 37069 · Faculty/Division: Temerty Faculty of Medicine · Department: Department of Nutritional Sciences · Campus: St. George (Downtown Toronto) · Position Number: · Description: · About us: · Home to over 40 departments and institutes, the Univer ...
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Research Coordinator
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CB Canada Toronto, CanadaOpportunity Awaits at Altus Group · The opportunity · Reporting to the Director, we are looking for a Research Coordinator to join our Data Solutions group. This is an exciting opportunity to launch your career in Real Estate, growing into a subject matter expert as part of a col ...
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Research Coordinator
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Research Coordinator
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Research Coordinator
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Research and Development Coordinator
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Research Study Coordinator
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Administrative Research Coordinator
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University Health Network Toronto, ON, CanadaThe University Health Network, where "above all else the needs of patients come first", encompassesToronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education. The breadth of researc ...
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Administrative Research Coordinator
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Senior Research Coordinator
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Research Coordinator 1
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Research Coordinator 2
Found in: Talent CA C2 - 4 days ago
Baycrest Toronto, CanadaThe Rotman Research Institute at Baycrest has an opportunity for a · Research Coordinator 2 · Position Type: Temporary Full-Time (1 Year) · Shift Type: Day · Bi-Weekly Hours: 70 Hours · Hours of Work: 7 hrs/shift · Posting Number: 7351 · Union: Non-Union · Date Posted: January 10 ...
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Senior Research Coordinator
Found in: Talent CA C2 - 5 days ago
Baycrest Toronto, Canada Full time/RegularResponsibilities include but are not limited to:Responsibilities include but are not limited to: Coordinates, monitors and supervises all study activities to ensure proper execution of assigned clinical research trials and to ensure that study protocols, SOPs, ICH-GCPs and regu ...
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Research Services Coordinator
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Research Coordinator 2
Found in: Talent CA C2 - 5 days ago
Baycrest Toronto, Canada TemporaryResponsibilities include but are not limited to:Responsibilities include but are not limited to: Serve as primary contact for multiple studies/sites · Recruit and screen patients for eligibility for current studies based on established protocols · Conducts and documents inform ...
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Research Ethics and Regulatory Coordinator
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Oak Valley Health Markham, Canada Temporary· Land acknowledgement: · Oak Valley Health honours the traditional territory of the closest Indigenous communities, the Chippewas (chi-puh-waas) of Georgina Island and the Mississaugas of Scugog Island. The Haudenosaunee (Ho-de-no-shau-nee) and Anishinaabe (Ah-nish-in-ah-beh) ...
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Research Ethics and Regulatory Coordinator
Found in: Talent CA C2 - 7 hours ago
Oak Valley Health Markham, Canada Full timeLand acknowledgement: · Oak Valley Health honours the traditional territory of the closest Indigenous communities, the Chippewas (chi-puh-waas) of Georgina Island and the Mississaugas of Scugog Island. The Haudenosaunee (Ho-de-no-shau-nee) and Anishinaabe (Ah-nish-in-ah-beh) have ...
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Research and Development Coordinator
Found in: Jooble CA O C2 - 3 days ago
pluscompany Toronto, ON, CanadaCitizen Relations is an international public relations agency with a well established UK presence. We create meaningful moments and impactful change that the world needs to see, authentically influencing brands into conversations in a way that matters. · And this approach has wo ...
Research Coordinator - Richmond Hill, Canada - Mackenzie Health
Description
Job Description
Research Coordinator Temporary Full-Time position (approximately 12 months)The Research Coordinator will work closely with the principal investigators to oversee all research activities, primarily in the Divisions of Critical Care and Neurology, Department of Medicine, and act as the liaison between Physicians, the Accelerating Clinical Trials (ACT) Consortium, participants, and study sponsors as needed.
Contribute to safe, quality care by
• Ongoing training for all active research protocols and amendments, in addition to the study delegation log for specified responsibilities;
• Recruiting study participants (., identifying and screening potential subjects, obtaining informed consent);
• Coordinating patient visit schedules as per study protocol, including ensuring ongoing informed consent;
• Executing or coordinating all aspects of study visits (., assessment of adverse events, monitoring safety, medication administration, sample collection, processing of samples according to clinical protocol);
• Reporting of adverse events and serious adverse events according to the Research Ethics Board, Sponsor, and Health Canada guidelines;
• Coordinating services for research requirements within Mackenzie Health (., laboratory, pharmacy, diagnostic imaging);
• Training and orientation healthcare staff to research studies;
• Completing Feasibility Questionnaires and Protocols for prospective new trials;
• Attending all site and study meetings as required;
• Actively working to support ACT initiatives, milestones, and deliverables, including participation in ACT meetings and discussions, and reviewing ACT protocols with physician champions and PI's as they become available
• Working autonomously to provide clinical research care for patients participating in clinical trials; liaising with other research teams or medical teams as needed; Contributing to a safe, inclusive environment for all through compliance with patient and staff safety policies and procedures.
• Assisting in drafting internal budgets for new and ongoing studies;
• Implementation and coordination of all aspects of data collection and source documentation, as per Mackenzie Health policy, ICH/GCP guidelines, and any applicable organizational policies.
What must you have?
• Bachelor's degree or higher level of education;
• Two years' experience working in research, including clinical trials is required.
What else do you bring?
• Excellent interpersonal, verbal and written communication skills;
• Attention to detail and meticulous documentation practice;
• Evidence of good physical assessment, psychosocial assessment and patient/family teaching skills;
• Experience with clinical data collection from electronic medical charts;
• Demonstrated proficiency with MS Office software – Word, Excel, Outlook and PowerPoint;
• Strong knowledge base in Clinical Trials including clinical research experience;
• Experience with grant and manuscript preparation and formatting;
• Knowledge of IATA shipping regulations and basic laboratory procedures;
• Ability to set priorities and work both independently and as a team member with accuracy in a dynamic, multidisciplinary environment;
• Willing to learn new research methodologies;
• Autonomous critical thinking ability;
• Excellent organizational and time management skills;
• Expected to work at both Mackenzie Health sites (Cortellucci Vaughan Hospital and Mackenzie Richmond Hill Hospital);
• Demonstrated behaviours consistent with Mackenzie Health's Commitment to Caring;
• Models behaviour that is aligned with the values of Mackenzie Health – Excellence, Leadership and Empathy;
• Commitment to providing exceptional experience for staff and clients within a challenging and exciting healthcare environment;
• Demonstrates understanding of contribution to patient and staff safety.
• Demonstrates strong decision-making, problem-solving and critical thinking skills.
Preferably, your profile also includes:
• A research-based Master's degree in a health-related field is strongly preferred.
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*You may be required to work at any site of Mackenzie HealthMackenzie Health is an inclusive and equal opportunity employer committed to providing accommodations for applicants upon request at any stage of the recruitment process in accordance with the Accessibility for Ontarians with Disabilities Act (AODA) and the Ontario Human Rights Code.