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WELL Health Technologies Corp
Overview
Perform medical screening tasks including obtaining informed consent, recording medical histories, and collecting biological samples in compliance with study protocols. Responsible for accurate data entry, vital signs monitoring, and ensuring regulatory compliance with GCP and SOPs.
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Compensation
CA$50,000 - CA$54,000 / YEAR
Posted
20 days ago
IQVIA
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
Inspired HR
The Clinical Research Dietician provides nutritional counseling and education to participants in dermatology, obesity, and metabolic clinical trials. They are responsible for implementing nutrition plans, monitoring participant adherence, and maintaining accurate regulatory documentation.
Salary not listed
28 days ago
Centricity Research
Support the execution of clinical research studies by recruiting participants and conducting study visits. Perform laboratory procedures including sample collection, processing, and shipping in compliance with protocols and SOPs.
Fortrea
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management. Ensures the protection of study patients and the integrity of data submitted on Case Report Forms.
1 month ago
Probity Medical Research Inc
The Source Worksheet Development Assistant is responsible for preparing data capture tools and performing administrative tasks for clinical trials. They must ensure regulatory compliance and maintain accurate study documentation within the company's online platform.
CA$25 - CA$25 / HOUR
The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.
CA$102,500 - CA$170,900 / YEAR
3 months ago
