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Bayshore
Overview
Administer and monitor specialized pharmacological treatments and investigational medicinal products in home, clinic, or community settings. Ensure strict adherence to clinical trial protocols, regulatory requirements, and accurate documentation of patient data.
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Compensation
Salary not listed
Posted
10 days ago
Translational Research in Oncology
Responsible for processing and quality reviewing study documentation for the electronic Trial Master File (eTMF) according to SOPs and GCP guidelines. Provides administrative support to the TMF Manager through reporting, metrics, and document metadata assignment.
CA$37,000 - CA$41,000 / YEAR
15 days ago
Care Access
The Clinical Research Coordinator, RN conducts delegated clinical tasks and monitoring of research participants while ensuring strict adherence to Good Clinical Practices (GCP) and protocol compliance. Key duties involve patient coordination, obtaining informed consent, performing clinical procedures like blood draws and ECGs, and managing investigational products.
20 days ago
1 month ago
Everest Clinical Research
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
