Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Providence Healthcare
Overview
Coordinate clinical trials from start-up to closeout, supporting multiple Principal Investigators within a centralized research model. Manage participant recruitment, screening, and data integrity while ensuring strict adherence to regulatory and ethical standards.
Quick view →
Compensation
CA$32 - CA$47 / HOUR
Posted
9 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.
Salary not listed
14 days ago
IQVIA
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
