Jobs for tmf at Vancouver

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,...

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,...

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,...

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team in a fully remote capacity in Canada. You will maintain compliance and completeness of TMF documentation, support inspections, and collaborate with cross-functional study teams.The ideal candidate has 1–3 years in TMF management, knowledge of eTMF platforms (Veeva Vault,...

Alimentiv is seeking a detail-oriented TMF Coordinator to join our TMF Operations team in a fully remote capacity in Canada. You will maintain compliance and completeness of TMF documentation, support inspections, and collaborate with cross-functional study teams. The ideal candidate has 1–3 years in TMF management, knowledge of eTMF platforms (Veeva...

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...

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...

Join to apply for the Agile Project Manager (ServiceNow) role at TELUS Digital 1 day ago Be among the first 25 applicants Join to apply for the Agile Project Manager (ServiceNow) role at TELUS Digital Who We Are Welcome to TELUS Digital — where innovation drives impact at a global scale. As an award‑winning digital product consultancy and the digital...

DescriptionSite Activation Specialist with payment experience in Clinical Trials (Client Dedicated, Remote - CAN)Site Activation Specialist with payment experience in Clinical Trials (Client Dedicated, Remote - CAN)Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with...

Exciting opportunity for a Clinical Documentation Management Specialist in Canada, managing TMFs for clinical studies from a remote setting. Ensure that essential study documentation meets high standards. As a Trial Master Files Representative, you'll play a key role in supporting clinical research through comprehensive documentation practices. Your...

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...

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 CSA/SAM,...

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...

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...

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...

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 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...

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 Data Manager will lead and manage clinical studies, ensuring that data are collected, managed and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with applicable regulatory requirements, industry...