Research Coordinator I Clinical Research Program
Unity Health Toronto —Toronto, ON
- Temporary
- Remote
- Customer service
- Microsoft Office
- Databases
9d
Project Coordinator - Term
CAGBC —Vancouver, BC
- $52,000–$58,000 a year
- Contract
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Paid time off
- Work from home
Quick apply
Junior Research Coordinator
Arthritis Research Canada —Vancouver, BC
- From $27.79 an hour
- Part-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Dental care
- Life insurance
Quick apply
Project Coordinator II-Canada
Indero —Remote
- Remote
- Bilingual
- Medication administration
- English
- Dental care
- Vision care
Quick apply
Project Coordinator
McLean & Company —Toronto, ON
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
11d
Senior Environmental Coordinator (Archaeology)
BC Hydro —Burnaby, BC
- $109,700–$138,700 a year
- Full-time
- Hybrid work
- Master's degree
- Analysis skills
- Bachelor's
Environmental Senior Field Coordinator
SynergyAspen Environmental —Fort St. John, BC
- $38–$47 an hour
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Profit sharing
- Work from home
Quick apply
13d
Environmental Senior Field Coordinator
SynergyAspen Environmental —Fort St. John, BC
- $38–$47 an hour
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Profit sharing
- Work from home
Quick apply
13d
Coordinators, Science and Research Branch
Ministry of Natural Resources —Sault Ste. Marie, ON
- $90,700–$133,653 a year
- Temporary
- Remote
- Bilingual
- Management
- English
6d
Impact Assessment Coordinator
SYSTRA —Montréal, QC
- Remote
- Bilingual
- PMP
- Writing skills
Coordinator, Environmental Services
Defence Construction Canada —Oromocto, NB
- $80,886–$105,152 a year
- Bilingual
- Engineering
- Business development
- Disability insurance
- Dental care
11d
Environmental Project Coordinator
GHD —Edmonton, AB
- Hybrid work
- Microsoft Excel
- Writing skills
- Engineering
Environmental Project Coordinator
360 ENGINEERING & ENVIRONMENTAL —Calgary, AB
- $75,000–$95,000 a year
- Full-time
- Hybrid work
- Engineering
- Bachelor's
- Organizational skills
- Flexible schedule
Quick apply
Environmental Project Coordinator
360 Engineering & Environmental Consulting Ltd. —Fort St. John, BC
- $75,000–$95,000 a year
- Full-time
- Hybrid work
- Engineering
- Data analysis skills
- Bachelor's
- Wellness program
- Disability insurance
Quick apply
5d

More jobs to discover

Find similar jobs that you might be interested in.

Project Coordinator
Applied Pharmaceutical Innovation —Edmonton, AB
Maintain comprehensive project documentation, including contracts, change orders, permits, project drawings, ensuring compliance with regulations.
$75,000–$90,000 a year
Project Coordinator - Term
CAGBC —Vancouver, BC
Support business development efforts as requested, including coordinating proposal documents, partner letters and budgets Financial and Contract Monitoring·…
$52,000–$58,000 a year
Quick apply

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Water Wastewater Compliance Coordinator
MISSISSAUGA'S OF SCUGOG ISLAND FIRST NATION —Port Perry, ON
Assists with the development and implementation of action plans addressing audit findings and non conformances and helps ensure all personnel are informed of…
$35.48–$40.59 an hour
Quick apply
Research Site Coordinator
Fleming College —Lindsay, ON
Completion of a four (4) year degree or three (3) year diploma/degree plus professional certification or equivalent in Analytical Chemistry, Organic Chemistry,…
$43.61–$50.39 an hour
1d

Show more jobs in cities nearby

I want to receive the latest job alerts for research coordinator in remote, canada

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

research coordinator jobs near remote, canada

Project Coordinator jobs in Ottawa, ON

Project Coordinator jobs in Toronto, ON

Environmental Project Manager jobs in Calgary, AB

Environmental Project Manager jobs in Edmonton, AB

Junior Software Developer jobs in Victoria, Bc

Research Assistant jobs in Vaughan, On

Automotive Sales Manager jobs in Calgary, Ab

Junior Research Manager jobs in Edmonton, Ab

Research Veterinary Technician jobs in Ontario

Aviation Manager jobs in Calgary, Ab

Supply Chain Manager jobs in Toronto, On

Clinical Manager jobs in Ontario

Remote Registered Nurse Case Manager jobs in Ontario

Research Coordinator jobs in London, On

Research Coordinator jobs in Edmonton, Ab

Clinical Research jobs in Guelph, On

Program Coordinator jobs in Remote

Research Assistant jobs in University Of Alberta (edmonton), Ab

Facilities Coordinator jobs in Ottawa, On

Research Coordinator jobs in Vancouver, Bc

Research Coordinator I Clinical Research Program

Unity Health Toronto -
Toronto, ON

Apply Now

Job details

Temporary | Full-time
9 days ago

Qualifications

Computer operation
Customer service
Filing
Microsoft Office
Databases
Bachelor's
Computer skills
Communication skills

Full job description

Research Coordinator I

The Research Institute is currently looking for a dynamic team player with excellent skills and experience in regulated clinical trials to fill an exciting new position as a Research Coordinator I.

Working within a newly established central clinical research unit, the position supports the efficient start-up, execution, and close-out of industry-sponsored clinical trials in compliance with Good Clinical Practice, Health Canada regulations, Division 5 of the Food and Drug Regulations, and institutional policies. The position will initiate new and support ongoing studies, including screening and recruiting eligible patients, obtaining informed consent, performing protocol-defined procedures, and accurately record study data in accordance with regulatory and quality standards.

The successful candidate will coordinate study activities across multiple investigators and clinical teams, standardizing workflows, supporting ethics and regulatory submissions, and ensuring accurate data collection and reporting. The position collaborates closely with sponsors and internal stakeholders to facilitate timelines, recruitment, and protocol adherence, while contributing to the development of streamlined processes and quality oversight within a growing centralized research infrastructure.

Additionally, the candidate will be responsible for providing administrative support including tracking and administering study related payments, maintaining appropriate inventory for study supplies, maintaining current lab licenses, freezer/drug logs and training certificates.

This position is full-time onsite with the option for occasional remote work.

Don’t meet every single requirement? Studies have shown that people in underrepresented communities are less likely to apply to jobs when they don’t meet every single qualification. We are dedicated to building an inclusive workplace, so if you’re excited about this role but your past experience doesn’t align perfectly, we still welcome you to apply.

Duties & Responsibilities:

Administrative Duties (50% of work time)

Creates trainings, manuals, e-learning content as needed.
Organizes, facilitates, and runs meetings with internal teams, and external stakeholders.
Facilitates the communication plan for internal and external stakeholders. Disseminates information as needed.
Ensures maintenance, collection, transcription, and entry of study related data, in accordance with hospital and privacy regulations.
General office duties e.g., filing, mailings, courier services, ensuring stocked and maintained inventory /supplies/equipment/software.
Designs all source documents (templates, tracking files, forms, guidance documents) for the collection, and management of information/data.
Organizes, sets up, and maintains equipment used in clinical research studies.
Provides high quality customer service experience when working with sponsors and external parties.

Research Specific Tasks (40% of work time)

Assists Principal Investigators and Research Program Manager in the initiation of new industry sponsored clinical trials and:
Coordinates and conducts screening, recruitment, and follow-up visits with participants.
Manages, prepares, and oversees monitors/audits.
Monitors, and controls research regulations, quality, and guidelines, including ethical (e.g., REB submissions), and safety protocols.
Writes and administers informed consent forms.
Arranges timely payments to participants.
Plans, organizes, directs, controls, and evaluates the activities and operations of research trials.
Liaises with multiple internal and external stakeholders at local and international levels, navigates stakeholder relationships, and responds proactively to anticipated challenges.
Helps develop processes, tools (workflow, Gantt charts), and resources to support team members, and projects.
Troubleshoots/solves logistical and technical obstacles.
Biological sample collection (Phlebotomy, dry blood spot testing etc.), processing and shipping according to Transportation of Dangerous Goods (TDG) and International Air Transport Association (IATA)
Maintains awareness of health and research news, events, and current high-profile research activities.

Day to day project and staff guidance tasks (10% of work time)

May train, coordinate, and/or delegate tasks (including overseeing quality control of submitted assignments) to Research Assistants, casual staff, students and internal/external collaborators.
May develop and implement policies, standards and procedures for the clinical trials and research operations in the department.

Performs cross functional and other duties as assigned and/or requested.

All staff are expected to carry out their assigned duties and responsibilities in a manner which prioritizes patient and employee safety, and confidentiality. Key accountabilities in this regard include:
Strict compliance with patient/employee confidentiality practices and policies.
Strict compliance with patient/employee safety practices and standards.
Appropriate identification, reporting and response to patient/employee confidentiality breaches in accordance with established policies and procedures.
Appropriate identification, reporting and response to patient/employee safety risks and incidents/events in accordance with established policies and procedures.

Qualifications:

Undergraduate Degree (Health Sciences preferred) and 2 years of relevant experience, OR demonstrable equivalent combination of specialized education and experience.
Experience with regulated clinical drug trials is preferred.
TCPS CORE 2, Good Clinical Practice and Health Canada Div 5 certificates are an asset. (Completed within first 2 weeks of hire)
Experienced phlebotomist with workshop certificate is an asset.
Completed a Clinical Research Academic Certificate Program is preferred
Clinical research professional designation is an asset (e.g., SOCRA, ACRP etc.).
Basic understanding of science, including applicable theories, frameworks, and models.
Excellent project coordination and problem solving skills.
Experience working with a diversity of stakeholders is an asset.
Empathy and ability to cope with emotionally difficult situations participants may be facing.
Basic computer skills with Microsoft Office experience, and database software (electronic data capture such as REDCap or Medidata).
Ability to work independently and as part of a team
Organization skills and ability to manage multiple projects simultaneously.
Excellent communication skills and strong interpersonal agility is an asset

Unity Health Toronto is committed to creating an accessible and inclusive organization. We strive to provide a recruitment process that is barrier-free and in compliance with the Accessibility for Ontarians with Disabilities Act (AODA) and the Ontario Human Rights Code. We understand that you may require an accommodation at any stage of the recruitment process. When you are contacted, please inform the Talent Acquisition Specialist and we will work with you to meet your accommodation needs. We want to emphasize that all accommodation requests are handled with the utmost confidentiality, respecting your privacy and dignity.

Apply Now

Refine Your Search

research coordinator jobs in remote, canada

Research Coordinator I Clinical Research Program

Project Coordinator - Term

Junior Research Coordinator

Project Coordinator II-Canada

Project Coordinator

Senior Environmental Coordinator (Archaeology)

Environmental Senior Field Coordinator

Environmental Senior Field Coordinator

Coordinators, Science and Research Branch

Impact Assessment Coordinator

Coordinator, Environmental Services

Environmental Project Coordinator

Environmental Project Coordinator

Environmental Project Coordinator

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alerts for research coordinator in remote, canada

Explore jobs in more locations

Research Coordinator I

Job seeker tools

Employer Tools

Browse

Stay Connected