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ICON plc
Overview
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.
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Compensation
Salary not listed
Posted
3 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
Alimentiv
Manage Trial Master File (TMF) content and processes throughout the study lifecycle from setup to archiving. Ensure the TMF is inspection-ready by performing periodic reviews, reconciling document lists, and collaborating with cross-functional study teams.
22 days 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
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
