Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
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.
Quick view →
Compensation
CA$60,000 - CA$90,000 / 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
Jobgether
Support regulatory affairs and patient safety activities, including labeling operations, submissions, and compliance documentation. Collaborate with global cross-functional teams to ensure adherence to international regulatory and pharmacovigilance standards.
Salary not listed
3 days ago
Johnson & Johnson Innovative Medicine
Develops and coordinates clinical and regulatory documents, including protocols and clinical study reports, within the oncology therapeutic area. Collaborates with cross-functional teams to establish document timelines and ensure adherence to internal standards and regulatory guidelines.
CA$74,000 - CA$119,600 / YEAR
4 days ago
ICON plc
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately conducted, recorded, and reported according to SOPs and ICH-GCP standards.
CA$108,576 - CA$135,720 / YEAR
17 days ago
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately recorded and reported in accordance with ICH-GCP and standard operating procedures.
Monitor the progress of clinical studies at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. Maintain accurate records and reports in accordance with ICH-GCP and standard operating procedures.
Centricity Research
The Clinical Research Coordinator will support study execution by performing clinical procedures, managing participant safety, and ensuring compliance with protocols and regulatory requirements. They will also handle recruitment, screening, and data documentation to maintain high standards of study integrity.
1 month ago
