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Jobgether
Overview
Serve as the primary contact for clinical trial sites to ensure protocol adherence and high-quality study execution from initiation to close-out. Conduct site visits and remote monitoring to maintain data integrity and ensure compliance with regulatory guidelines.
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Compensation
Salary not listed
Posted
3 days ago
Canadian Mental Health Association- Peel Branch
Provide addiction services including screening, assessment, and monitoring of anti-craving medications within a multidisciplinary team. Collaborate with providers to support clients in crisis and manage psychopharmacologic treatment plans.
CA$75,509 - CA$89,160 / YEAR
7 days ago
Health Sciences North Research Institute
Oversee and manage clinical research studies across multiple portfolios from start-up to close-out. Coordinate day-to-day operations, data collection, and participant recruitment while ensuring regulatory compliance.
CA$31 - CA$37 / HOUR
11 days ago
Worldwide Clinical Trials
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
14 days ago
IQVIA
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
CA$84,000 - CA$170,900 / YEAR
17 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
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
