tmf

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...

Job Title: TMF Associate Employment Type: Full time, Permanent Job Reports To: Manager, TMF Operations Department/Unit Name: TMF Operations Job Summary: Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study set up to transfer/archiving. Work in partnership with study...

We are seeking a detail-oriented and highly organizedTMF Coordinatorto 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...

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...

Join our TMF Operations team as a TMF Associate, dedicated to successful Trial Master File management. Enjoy a remote work environment while ensuring TMF compliance and integrity.In this full-time role, the TMF Associate is essential in managing the TMF content from initiation to archiving. You’ll work closely with study teams to address TMF-related...

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,...

Become a TMF Operations Coordinator, responsible for the quality and compliance of Trial Master Files. Your detail-oriented skills will ensure our documentation meets rigorous standards.In this role, you will maintain the completeness and compliance of TMF documentation crucial for clinical trials. Collaborating with study teams, you will manage essential...

Join our TMF Operations team as a TMF Associate, dedicated to successful Trial Master File management. Enjoy a remote work environment while ensuring TMF compliance and integrity.In this full-time role, the TMF Associate is essential in managing the TMF content from initiation to archiving. You'll work closely with study teams to address TMF-related...

Elevate your career as a TMF Associate at a leading organization managing the Trial Master File. This full-time opportunity focuses on meticulous TMF management processes.As a TMF Associate, you will be responsible for overseeing TMF content throughout the study lifecycle. Collaborate with study teams regularly and ensure the TMF remains complete and...

Elevate your career as a TMF Associate at a leading organization managing the Trial Master File. This full-time opportunity focuses on meticulous TMF management processes.As a TMF Associate, you will be responsible for overseeing TMF content throughout the study lifecycle. Collaborate with study teams regularly and ensure the TMF remains complete and...

**Job Title:**  TMF Associate **Employment Type:** Full time, Permanent **Job Reports To** : Manager, TMF Operations **Department/Unit Name** : TMF Operations **Job Summary:** Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study set up...

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...

- Analyze, question, and improve how clinical trial work is done while meeting business objectives through efficient, quality trial execution from startup to closeout - Execute core clinical operations activities, including site management, SIV, IMV, closeout visits, and Trial Master File (TMF) maintenance - Participate in reviews of site contracts, budgets,...

OverviewWe are seeking a highly skilled and visionary ServiceNow Architect with deep expertise in Proactive Service Experience (PSE), Order Management for Telecommunications (OMT), and Hardware Asset Management (HAM) modules. The ideal candidate will bring a strong background in the telecommunications industry, with a solid grasp of TM Forum (TMF)...

We never ask for payment as part of our selection process, and we always contact candidates via our corporate accounts and platforms. If you are approached for payment, this is likely to be fraudulent. Please check to see whether the role you are interested in is posted on our career website. About TMF Group TMF Group is a leading provider of employee,...

Worldwide Clinical Trials is seeking a Clinical Research Associate in Canada. You will manage site activities across multiple therapeutic areas, including oncology, with remote site management and regional travel supporting regulatory submissions and TMF processes. The role requires 5+ years as a CRA, a 4-year degree or nursing degree, and the ability to...

Profound Medical is seeking a Clinical Research Associate to analyze and improve trial execution from startup to closeout. You will manage site visits, adapt to protocol changes, and ensure TMF integrity, while maintaining strong relationships with study personnel. The role requires a Bachelor’s in biomedical sciences (MSc preferred), and certifications...

Syneos Health is seeking a bilingual Clinical Research Associate for sponsor-dedicated, home-based work in Quebec, Canada. The role involves remote monitoring, site management, and ensuring regulatory and protocol compliance across trials. You will support ISF/TMF review, IP handling, and sponsor communications to drive study success. The candidate must be...

Chez Allucent™ nous nous engageons à aider les petites et moyennes entreprises biopharmaceutiques à naviguer efficacement dans l’univers complexe des essais cliniques afin d’offrir des traitements qui changent la vie aux patients qui en ont besoin partout dans le monde. At Allucent™, we are dedicated to helping small-medium biopharmaceutical...