tmf 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...

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...

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...

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...

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...

Alimentiv is seeking a TMF Coordinator to maintain quality and compliance of Trial Master File documentation, ensuring inspection readiness and alignment with ICH-GCP and FDA/EMA expectations. You will file, index, and manage TMF content across eTMF systems like Veeva Vault, Phlexglobal, and Trial Interactive, while collaborating with study teams and QA to...

Join a dynamic team as a Trial Master File Associate, managing TMF content for study life cycles in a hybrid working environment. Ensure compliance and organization in TMFs while interacting with cross-functional teams. This full-time TMF Associate role focuses on managing content from study setup to archiving. You'll work closely with study teams during...

ICON Strategic Solutions in Montreal is seeking a Sr. Site Management Associate (French Speaking) to oversee sponsor-dedicated site operations during enrollment and maintenance, leveraging ICON's global expertise.You will collaborate with PIs and study coordinators, ensure TMF readiness, and guide sites on sponsor systems such as IRT, EDC, eTMF, and CTMS...

Parexel FSP in Canada seeks a Global Site Start-up Lead responsible for global execution of site activation for assigned trials, ensuring efficiency, timeliness, and compliance with SOPs and ICH/GCP. This role partners with CROs and internal teams to drive cross-functional collaboration.You will lead site start-up strategy, country start-up planning,...

Parexel FSP is looking for Global SSU Lead to join our team in Canada! Job Overview The Global Site Start-up (SSU) Lead is accountable for the global execution of site activation for assigned clinical trials, performing responsibilities with moderate oversight. The Global SSU Lead is accountable for ensuring site start-up is efficient, timely and in...

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Project Manager II, Early Phase based in Canada. Are you an experienced clinical research professional ready to lead complex early-phase clinical trials from initiation through closeout? This role offers the opportunity to...

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...

Lead clinical site activation across Canada using regulatory expertise, CTMS knowledge, and precise document management for Parexel FSP trials. This remote role serves regional sites.As a Regional Site Start Up II, you will deliver activation activities across clinical trials and address geographic-specific needs. You will coordinate essential documents,...

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...

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 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 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...

Join our TMF Operations team as a TMF Coordinator focused on ensuring quality and compliance in Trial Master File documentation. This role supports clinical trials through effective document management and collaboration. We're seeking a detail-oriented TMF Coordinator to manage TMF documentation adhering to global regulations. Your responsibilities will...

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...