tmf assistant jobs in 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...

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 theTMF. Manage access and organization of the controlled electronic file repository, in...

We are seeking a detail-oriented and highly organized TMF Coordinator to join our TMF Operations team. In this role, you will be responsible for maintaining the quality, completeness, and compliance of Trial Master File (TMF) documentation in alignment with global regulatory requirements and company standards. You will play a key role in ensuring that TMF...

Parexel FSP is looking for Regional Site Start Up II to join our team in Canada. Job Summary The Regional Site Start Up (SSU) role is responsible for leading and delivering site start-up and activation activities across clinical trials. This role will ensure timely site activation, maintain strong relationships with sites, and work cross-functionally with...

Sr. Site Management Associate (French Speaking) At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...

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, 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...

External Job Description Key Accountabilities: Clinical Trial Site Activation: Initiate and coordinate activities and essential documents management during start up towards the compilation of a high quality Investigator Initiation Package (IIP) leading to approval for site initiation Provide support to resolve issues or concerns and timely escalation of...

The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key responsibility of a CRA is as a site...

Site Activation Specialist II Remote in Canada-QC-Montreal (Client Dedicated) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and...

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...

Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the McGill University Health Centre (RI-MUHC), you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and...

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...

Senior Clinical Research Associate (Sr. CRA) ABOUT THE ROLE Thryv Therapeutics is a clinical-stage biopharmaceutical company headquartered in Montreal, Canada, developing therapies for cardiovascular diseases. As a lean, fast-moving start-up, we are building our clinical operations function from the ground up, which means this role carries important...

We are seeking a detail-oriented and highly organized TMF Coordinator to join our TMF Operations team. In this role, you will be responsible for maintaining the quality, completeness, and compliance of Trial Master File (TMF) documentation in alignment with global regulatory requirements and company standards. You will play a key role in ensuring that TMF...

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

Assistant(e) chargé(e) de projet clinique - Phase I à IV Position ouverte aux citoyens/résidents canadiens ou détenteurs de permis de travail canadien Temps complet Seriant, une division de l’Institut de cardiologie de Montréal, est une organisation de recherche clinique qui offre des services complets à l’industrie pharmaceutique et...

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...

Sr. Site Management Associate (French Speaking)At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...

Sr. Site Management Associate (French Speaking)At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of...