etobicoke, on clinical data coordinator Jobs – 34 Openings This Week

Clinical Research Coordinator (RN)
Cardio Health Inc. —Mississauga, ON
- $27–$30 an hour
- Part-time
- Microsoft Powerpoint
- Microsoft Word
- CPR Certification
- Dental care
Quick apply
Director, Patient Recruitment & Retention
WELL Health Technologies Corp —Toronto, ON
- $110,000–$130,000 a year
- Full-time
- Microsoft Office
- Computer skills
- Leadership
Quick apply
Lab Technician (Casual) - Shift Work Available
ClinSurge Research —Toronto, ON
- Laboratory experience
- Bachelor's
- Associate's degree
Quick apply
Manager of Informatics/RAI Lead
Cooksville Care Centre —Mississauga, ON
- $75,000 a year
- Supervising experience
- Computer skills
- Communication skills
Quick apply
7d
Research Analyst - Institute for Mental Health Policy Research
CAMH —Toronto, ON
- $27.95–$37.28 an hour
- Part-time
- Data analysis skills
- Research
- Databases
4d
Research Assistant / Laboratory Specialist
Centricity Research —Vaughan, ON
- $21–$25 an hour
- Full-time
- Microsoft Office
- Designated paid holidays
- Dental care
Quick apply
Research Analyst - Centre for Youth Bipolar Disorder
CAMH —Toronto, ON
- $27.95–$37.28 an hour
- Full-time
- Bachelor's
- Psychology
- Organizational skills
1h
Senior Clinical Research & Medical Affairs Specialist
Mimosa Diagnostics —Toronto, ON
- Full-time
- Hybrid work
- Nursing
- Microsoft Excel
- Master's degree
- Dental care
- Vision care
Quick apply
10d
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-16108
Sunnybrook Health Sciences Centre —Toronto, ON
- Master's degree
- Psychology
- Organizational skills
Quick apply
Student (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2026-17307
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporary
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Post-Doctoral Research Fellow in Neuroimaging
SickKids —Toronto, ON
- From $54,000 a year
- Doctoral degree
- Computer Science
- Engineering
- Dental care
Bench Supervisor (Microbiology) - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins Canada BioPharma —Toronto, ON
- $65,000 a year
- Overtime
- Doctoral degree
- Laboratory experience
- Microsoft Office
- Designated paid holidays
- Disability insurance
Quick apply

More jobs to discover

Find similar jobs that you might be interested in.

Senior Director, Specialty Programs
Specialty Health Network Inc. —Mississauga, ON
Build & execute program and client-level plans to drive best-in-class results and program profitability. As an active member of the SHN Leadership team, play a…
$170,000–$220,000 a year
6d
Director, Patient Recruitment & Retention
WELL Health Technologies Corp —Toronto, ON
Work with Marketing department to create strategies to maximize reach, engagement, and conversion of new study participant using digital marketing, social media…
$110,000–$130,000 a year
Quick apply

Show more similar jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Clinical Research Coordinator
MyHealth Partners Inc. —Scarborough, ON
Bachelor's degree in health-related field required, Master's degree is an asset. Recognized certification in clinical research (ACRP or SOCRA) is an asset.
$100,000–$120,000 a year
Quick apply
Lab Technician (Casual) - Shift Work Available
ClinSurge Research —Toronto, ON
Associate’s or Bachelor’s degree in Biology, Chemistry, Medical Laboratory Science, or related field. Collaborate closely with clinical coordinators, research…
Quick apply

Show more jobs in cities nearby

I want to receive the latest job alerts for clinical data coordinator in etobicoke, on

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

clinical data coordinator jobs near etobicoke, on

Director Of Recruiting jobs in Toronto, ON

Laboratory Technician jobs in Toronto, ON

Clinical Evaluator jobs in Toronto, ON

Microbiology Supervisor jobs in Toronto, ON

Clinical Research Coordinator jobs in Mississauga, ON

Clinical Research Coordinator jobs in Toronto, ON

Research Analyst jobs in Toronto, ON

Director Of Recruiting jobs in Ontario

It Audit Director jobs in Toronto, On

Director Of Finance jobs in Vancouver, Bc

Director Of Development jobs in Calgary, Ab

Child Care Director jobs in Toronto, On

Clinical Research Specialist jobs in Calgary, Ab

Undergraduate Research jobs in Edmonton, Ab

Clinical Research Specialist jobs in Ontario

Disability Accommodation Specialist jobs in Ontario

Clinical Psychologist jobs in Ontario

Clinical Research Specialist jobs in Toronto, On

Non Clinical Nursing jobs in Vancouver, Bc

Clinical Research Specialist jobs in Greater Toronto Area, On

Clinical Research Coordinator (RN)

Cardio Health Inc. -
Mississauga, ON

Quick apply

Job details

Permanent | Part-time | Full-time
$27–$30 an hour

Qualifications

Microsoft Powerpoint
Microsoft Word
CPR Certification
Microsoft Excel
Laboratory experience
Research
Microsoft Office
CNO Membership
Analysis skills
First Aid Certification
Recruiting
Organizational skills
Medical terminology
Communication skills

Full job description

Cardio Health Clinical Trials (CHCT) is a site management organization with over a decade of experience in managing and conducting clinical trials across multiple therapeutic areas, specializing in Cardiovascular and Gastroenterology. With multiple investigator sites across Ontario, CHCT is committed to delivering personalized services with a team of qualified experts.

Position Summary

The Clinical Research Coordinator (CRC) plays a pivotal role in supporting, facilitating, and coordinating the day-to-day clinical trial activities under the direction of the Principal Investigator (PI). The CRC ensures the seamless execution of clinical trials while adhering to Good Clinical Practice (GCP) guidelines and regulatory standards. This role requires close collaboration with the Clinical Trial Manager, study sponsors, and institutional stakeholders.

Key Responsibilities

General Responsibilities

· Conduct clinical research studies in compliance with the study protocol, Good Clinical Practice (GCP), and CHCT Research SOPs.

· Participate in clinical trial activities, including pre-screening, screening, informed consent procedures, randomization, administration, vital signs and ECG recording, visit coordination, sampling, and scheduling.

· Maintain regulatory documentation and study-specific logs.

· Ensure timely and accurate transcription of data into source documents, paper case report forms, and electronic CRFs.

· Proficiently perform phlebotomy and handle biological sample processing.

· Travel to attend research and investigator meetings as required.

· Participate in monitoring visits, investigator meetings, site initiation visits, closeout visits, and audits.

· Manage package drops and pickups (e.g., Amazon, FedEx) to ensure study materials and samples are available and handled promptly.

Participant Engagement

· Recruitment: Identify, screen, and enroll eligible study participants while obtaining informed consent.

· Visit Coordination: Schedule patient visits as per protocol and maintain adherence to study timelines.

· Participant Interaction: Conduct study visits, assess adverse events, monitor safety, and collect biological samples.

Operational Support

· Study Compliance: Maintain accurate, up-to-date study binders and ensure adherence to regulatory requirements.

· Sample Handling: Collect, process, label, store, and ship biological specimens in line with protocol requirements.

· Equipment Oversight and Training:

o Conduct routine checks to ensure research equipment is functional.

o Train and operate trial-specific equipment, including cardiology diagnostic tools and specialized devices.

o Promptly report and address equipment-related issues.

· Package Management: Handle the pickup and delivery of study materials and samples efficiently.

Site Management

· Serve as a backup CRC at other CHCT sites as needed.

· Coordinate with team members to ensure seamless site operations and coverage.

QualificationsEducation

· You must hold a current certification of registration from the College of Nurses of Ontario and maintain membership with the RPNAO or RNAO.

Certifications

· Good Clinical Practice (GCP) certification (essential).

· Certifications from SOCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) are highly preferred.

· Phlebotomy certification is required.

· [NR1] CPR/First Aid certificate an asset

Experience

· 2-3 years of experience in clinical trials, research coordination, or related clinical roles (Phase 1-4 clinical trial experience is an asset).

· Infusion experience (e.g., IV insertion, IV drug administration, infusion monitoring)

· Experience in patient recruitment, informed consent, and patient visit coordination.

· Proficiency in biological sample collection, handling, and processing.

· Experience working in hospital or clinic settings for 2-3 years.

· Familiarity with electronic data capture systems and trial master files (TMFs).

Skills

· Experience in Physical Assessment: Proficient in medical terminology and capable of taking vital signs (BP, RR, temperature, etc.).

· Communication Skills: Excellent verbal and written communication for interactions with patients, sponsors, and research teams.

· Organizational Skills: Strong multitasking ability with exceptional attention to detail and accurate record-keeping.

· Regulatory Knowledge: Familiarity with Health Canada and FDA regulations relevant to clinical trials.

· Technical Proficiency: Competency in clinical trial management systems (CTMS) and MS Office Suite (Word, Excel, PowerPoint).

· Knowledge of IATA Shipping Regulations and Basic Laboratory Procedures: Ensures proper handling and transport of biological samples.

· Flexibility and Teamwork: Capable of working independently with minimal supervision and collaborating within a team environment.

· Problem-Solving and Analytical Skills: Ability to identify and resolve issues effectively.

Other Requirements

· Availability to work beyond standard business hours, including evenings and weekends, if required by the study protocol.

· Ability to travel between research sites when necessary.

· Access to reliable transportation for site visits and package deliveries.

· Adherence to professional appearance and conduct, following a business casual dress code or study-specific guidelines.

CPR/First Aid certificate an asset

Pay: $27.00-$30.00 per hour

Benefits:

Dental care
Extended health care

Application question(s):

Outline your clinical trial experience
Describe your experience with patient history taking
4. Provide examples of your organizational skills

Licence/Certification:

Registered Nurse License (required)

Work Location: In person

Quick apply

Refine Your Search

clinical data coordinator jobs in etobicoke, on

Clinical Research Coordinator (RN)

Director, Patient Recruitment & Retention

Lab Technician (Casual) - Shift Work Available

Manager of Informatics/RAI Lead

Research Analyst - Institute for Mental Health Policy Research

Research Assistant / Laboratory Specialist

Research Analyst - Centre for Youth Bipolar Disorder

Senior Clinical Research & Medical Affairs Specialist

Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-16108

Student (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2026-17307

Post-Doctoral Research Fellow in Neuroimaging

Bench Supervisor (Microbiology) - Eurofins BioPharma Product Testing Toronto, Inc.

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alerts for clinical data coordinator in etobicoke, on

Related Searches

Explore jobs in more locations

Job seeker tools

Employer Tools

Browse

Stay Connected