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The Memory ClinicNew
Overview
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.
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Compensation
CA$60,000 - CA$90,000 / YEAR
Posted
New
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
Rejuvenation
Coordinate all clinical trial activities in compliance with protocols and regulatory requirements. This includes recruiting participants, conducting research visits, and maintaining accurate study documentation using the RealTime CTMS system.
14 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
