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Medix™

Clinical Research Coordinator

Cambridge, ON, Canada

Full-time

Within 25 km of Guelph · About 14.9 km from the city centre

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Job details

Job type: Full-time
Apply by: Nov 19, 2026
Posted: Oct 20, 2026

Original job description

Open to CRCs or CRNs

Therapeutic area: Cardiac

POSITION SUMMARY:

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Duties and Responsibilities:

Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s

Adhere to Good Clinical Practices and the study protocols

Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials

Discuss study protocols with patients and verify the informed consent documentation Provide patient with written communication of their participation (i.e. copy of the signed informed consent)

Dispense study medication in a professional and accountable manner following protocol requirements

Perform ECGs and obtain vital signs of patients

Schedule all patient research visits and procedures consistent with protocol requirements

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More about this job

Responsibilities

Coordinate and administer approximately six to eight cardiac clinical trials, following research SOPs, Good Clinical Practices, and study protocols. Manage patient consent and communications, dispense study medication, perform ECGs and collect vital signs, and schedule research visits and procedures.

Requirements

The role requires the ability to manage clinical and administrative trial activities and apply sound judgment and detailed knowledge of study-specific protocols. It is open to Clinical Research Coordinators or Clinical Research Nurses; no education or years-of-experience requirements are specified.

Skills

Clinical Trial Coordination
Clinical Research Administration
Good Clinical Practices
Protocol Compliance
Informed Consent
Patient Communication
Study Medication Dispensing
Electrocardiograms
Vital Signs Measurement
Research Visit Scheduling
Data Integrity
Patient Safety

Visa sponsorship

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Keywords

Clinical Research Coordinator
Clinical Research Nurse
Cardiac
Clinical Trials
Research SOPs
Good Clinical Practices
Study Protocols
Scientific Integrity
Patient Rights
Patient Safety
Informed Consent
Study Medication
Electrocardiograms
ECGs
Vital Signs
Patient Visits
Clinical Research Administration
Trial Coordination

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