Jobs for tmf at Montreal

Base pay range CA$52,500.00/yr - CA$87,500.00/yr Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study setup to transfer/archiving. Work in partnership with study teams during periodic file reviews and audits to address findings related to the TMF. Manage access and organization...

The TMF Document Coordinator II plays a key support role in maintaining the Sponsor’s Trial Master File (TMF) throughout the duration of a clinical trial. The TMF Coordinator II reviews and processes TMF records through quality control workflows to ensure they meet required quality, compliance, and regulatory standards before being approved into the TMF,...

A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle. The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing TMF organization and regulatory compliance. Responsibilities include ensuring the TMF is complete and ready for...

The TMF Document Coordinator II plays a key support role in maintaining the Sponsor’s Trial Master File (TMF) throughout the duration of a clinical trial. The TMF Coordinator II reviews and processes TMF records through quality control workflows to ensure they meet required quality, compliance, and regulatory standards before being approved into the TMF,...

Base pay range CA$52,500.00/yr - CA$87,500.00/yr Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study setup to transfer/archiving. Work in partnership with study teams during periodic file reviews and audits to address findings related to the TMF. Manage access and...

Indero is seeking a TMF Document Coordinator II to support trial master file activities across Investigator-Initiated and limited-scale studies in Canada. The role focuses on TMF review, metadata classification and quality control to ensure regulatory compliance. You will collaborate with cross-functional teams, manage timelines, generate TMF metrics, and...

A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle. The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing TMF organization and regulatory compliance. Responsibilities include ensuring the TMF is complete and ready for...

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team. You will manage Trial Master File documentation to ensure compliance with ICH-GCP, FDA, and EMA standards and keep content inspection-ready across globally distributed trials.You will file, index, and control versions in eTMF systems (Veeva Vault, Phlexglobal, Trial...

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team. You will manage Trial Master File documentation to ensure compliance with ICH-GCP, FDA, and EMA standards and keep content inspection-ready across globally distributed trials. You will file, index, and control versions in eTMF systems (Veeva Vault, Phlexglobal, Trial...

Take on an essential role as a Trial Master Files Specialist for clinical research studies in Canada. This remote position focuses on maintaining accurate documentation and TMF organization.The Trial Master Files Representative collaborates with clinical research teams, project managers, and stakeholders to maintain essential study documentation. Your...

Syneos Health is seeking a Site Activation Specialist with payment experience in Clinical Trials for a Client Dedicated, Remote CAN role. You will manage country-level submissions, oversee site activation end-to-end, and coordinate regulatory communications with local authorities. Responsibilities include preparing EC and RA submissions, working with...

The Project Manager II, EPTR has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Trial Master Files Representative based in Canada.This remote role supports the accurate preparation, organization, and maintenance of Trial Master Files (TMFs) for clinical research studies. You’ll help ensure essential study...

Senior Project Manager, Early Phase and Translational Research (Sr. PM, EPTR) The Senior Project Manager, Early Phase and Translational Research (Sr. PM, EPTR) oversees and manages domestic, regional and/or international projects. The senior project manager is responsible for developing and managing project teams, communications, risk, scope, schedule,...

Don't see an opening that quite matches what you're looking for, or not ready to make a move yet? Let us know!We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the process looks like:  A Talent Acquisition...

The Project Manager II, EPTR has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable...

Line Manager, Regulatory Affairs, CRO, Canada remote, This role combines people leadership and operational delivery, actively contributing to the execution of clinical trial regulatory activities.As a Line Manager & Regulatory Affairs Specialist, the employee will be responsible of overseeing Ethics Committee (EC), Regulatory Authority (RA), and other...

Line Manager, Regulatory Affairs, Canada remote, This role combines people leadership and operational delivery, actively contributing to the execution of clinical trial regulatory activities.As a Line Manager & Regulatory Affairs Specialist, the employee will be responsible of overseeing Ethics Committee (EC), Regulatory Authority (RA), and other...

The Project Manager, Vendor Management ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. In addition to overall project coordination, the Project Manager plays a key role in the oversight and management of study-specific vendors throughout the project lifecycle, including...

The Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Project Manager I must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory and...