tmf assistant jobs in Toronto

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...

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,...

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...

Clinical Research Associate – Canada Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating clinical research and improving patient outcomes. Responsibilities Perform site qualification, initiation, interim monitoring, site management, and close‑out visits (on‑site or remote) ensuring compliance with...

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...

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 Operations Lead needs (COL & Sr. COL) to support our Clinical Monitoring team. What the process looks like: A Talent Acquisition representative will...

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...

CRA - Future roles (Canada)Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Every day we perform better because of how we work together, as one team, each the...

Sr Clinical Project Manager - Early PhaseSyneos 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 accelerate progress. Our Clinical...

Clinical Research Associate – Canada Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating clinical research and improving patient outcomes. Responsibilities Perform site qualification, initiation, interim monitoring, site management, and close‐out visits (on‐site or remote) ensuring compliance...

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,...