Clinical Research Associate
CanadaFull-TimeMiddle
SalaryBase salary + eligibility for performance-based bonus
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Job Details
- Experience
- Minimum 1 to 3 years depending on seniority level (CRA I: 1+ year, CRA II: 2+ years, Sr. CRA: 3+ years)
- Required Skills
- GCP
Requirements
- Honours Bachelor Degree
- Minimum 1 year of experience for CRA I
- Minimum 2 years of experience for CRA II
- Minimum 3 years of experience for Sr. CRA
- Knowledge of SOPs, protocol, and Good Clinical Practice (GCP)
- Familiarity with EDC, CTMS, RBM, and TMF systems
Responsibilities
- Support or conduct site management through remote and supervised onsite visits in compliance with SOPs, protocol, and GCP.
- Perform remote data and system reviews (EDC, CTMS, RBM, TMF) to ensure data quality and regulatory compliance.
- Assist or lead query resolution, safety reviews, and adverse event follow-up throughout the study lifecycle.
- Support or conduct site startup and activation activities, including investigator coordination and trial material delivery.
- Maintain accurate and complete TMF documentation.
- Provide operational support to Senior and Lead CRAs.
- Participate in training, study meetings, and professional development activities.
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