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ICON plcNew
Overview
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.
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Compensation
CA$110,520 - CA$138,150 / YEAR
Posted
New
The Memory ClinicNew
The Clinical Trial Associate manages regulatory tasks for Alzheimer's research trials, including IRB submissions and the maintenance of master files. They coordinate start-up activities and ensure ongoing compliance with ICH-GCP regulations and sponsor requirements.
CA$60,000 - CA$90,000 / YEAR
AstraZenecaNew
The CRA is responsible for monitoring study conduct at allocated sites to ensure proper delivery and compliance with international guidelines and local regulations. Key tasks include site initiation, monitoring visits, data verification, and managing study supplies and documentation.
CA$109,149 - CA$143,258 / YEAR
ICON plc
Accountable for site selection and study start-up activities for Phase I-IV trials, ensuring timelines and deliverables are met. Manages regulatory submissions, site documentation, and financial contracts to achieve site greenlight.
Salary not listed
3 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
8 days ago
Indero
The Senior CRA monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP guidelines. Responsibilities include conducting site visits, performing source data verification, and potentially mentoring other CRAs as a Lead CRA.
Coordinate the setup and monitoring of oncology clinical trials while maintaining accurate study documentation and reports. Build collaborative relationships with investigators and site staff to ensure patient safety and regulatory compliance.
15 days ago
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits to ensure clinical trials adhere to protocols and regulatory standards. They also build relationships with investigators, perform source data verification, and may mentor other CRAs while overseeing site metrics.
16 days ago
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately conducted, recorded, and reported according to SOPs and ICH-GCP standards.
CA$108,576 - CA$135,720 / YEAR
17 days ago
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately recorded and reported in accordance with ICH-GCP and standard operating procedures.
Monitor the progress of clinical studies at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. Maintain accurate records and reports in accordance with ICH-GCP and standard operating procedures.
Inspired HR
The Clinical Research Coordinator leads multiple concurrent clinical trials, ensuring strict protocol adherence and high-quality data delivery. They manage the entire patient lifecycle from screening and enrollment to follow-up assessments and data documentation.
22 days ago
ClinSurge Research
The coordinator manages clinical research studies by handling participant recruitment, consent, and data entry into EDC systems. They ensure strict compliance with GCP, Health Canada, and IRB regulations while collaborating with investigators and sponsors.
23 days ago
AstraZeneca
The Clinical Research Associate (CRA) is responsible for the local delivery of clinical studies at assigned sites, acting as the main contact for monitoring study conduct to ensure proper delivery according to guidelines and regulations. This involves preparing, initiating, monitoring, and closing assigned sites, training site staff, driving site performance, and ensuring data quality and compliance.
Everest Clinical Research
The Clinical Trial Assistant will interact with sponsors, sites, and vendors to ensure timely and high-quality operationalization of clinical trials while compiling and reviewing documentation for site qualification and regulatory submissions. Responsibilities also include setting up, maintaining, and archiving essential documents in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
CA$45,000 - CA$65,000 / YEAR
2 months ago
The Clinical Research Associate is locally responsible for study delivery at assigned sites, acting as the main contact to monitor study conduct, ensuring compliance with AZ procedures and international guidelines like ICH-GCP. Key tasks include preparing, initiating, monitoring, and closing sites, training site staff, driving site performance, and ensuring timely data quality and reporting.
3 months ago
Victoria
British Columbia
394 live openings
Surrey
386 live openings
Ottawa
Ontario
347 live openings
Saskatoon
Saskatchewan
346 live openings
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