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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
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
Headlands Research
Clinical Research Coordinators manage the day-to-day execution of clinical trials, including coordinating study visits and collecting data. They work directly with patients, investigators, and cross-functional teams to ensure compliance with protocols and regulatory requirements.
CA$45,000 - CA$100,000 / YEAR
9 days ago
Syneos Health
The Analytical Scientist I provides support for the routine analysis of biological samples and ensures all activities follow company policies and SOPs. Responsibilities include processing samples, documenting results, and assisting with laboratory maintenance and waste disposal.
Salary not listed
10 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
ICON plc
The Clinical Research Associate will monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also collaborate with cross-functional teams to manage data collection, site performance, and stakeholder relationships.
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
21 days ago
Coordinate clinical research studies by performing complex clinical procedures and managing subject well-being. Responsibilities include recruiting volunteers, administering study drugs, and ensuring data accuracy in accordance with protocols.
CA$40 - CA$50 / HOUR
25 days ago
CHARM Fertility
The Registered Practical Nurse will provide comprehensive nursing care, including medication administration and patient education, within a collaborative interdisciplinary team. They are responsible for managing patient treatment cycles, providing emotional support, and maintaining clinical standards in a fertility clinic setting.
CA$28 - CA$28 / HOUR
1 month 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
The Registered Practical Nurse will autonomously carry out clinical practice, providing evidence-based nursing care including medication administration, blood collection, and comprehensive patient education regarding treatment cycles and self-injections. Responsibilities also involve coordinating care, communicating with the interdisciplinary team, and providing essential emotional support and counselling to patients and their families.
3 months ago
SteriMax Inc.
The role involves supporting pharmacovigilance operations such as adverse event processing, literature review, signal detection, and PBRER preparation, while effectively utilizing custom Python-based automation tools and AI platforms to optimize workflows. Responsibilities also include running automated scripts, ensuring data quality, performing regulatory compliance checks, and collaborating with the PV team on daily operations.
4 months ago
