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Indero
Overview
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits to ensure clinical trials adhere to protocols and regulatory standards. They also build relationships with investigators, perform source data verification, and may mentor other CRAs while overseeing site metrics.
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Compensation
Salary not listed
Posted
16 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.
Sentrex Health Solutions
The Pharmacovigilance Associate manages the collection, processing, and reporting of adverse events and product complaints in compliance with regulatory requirements. They also assist with administrative tasks within the Quality Management System to ensure adherence to GxP standards.
CA$62,000 - CA$73,000 / YEAR
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 Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
CA$65,000 - CA$100,000 / YEAR
4 months ago
