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Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal

Montréal, QC
Hybrid
Posted Aug 28, 2026
1 position

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Employment type: Full-time
Experience level: Mid-level · 2+ years
Minimum education: Bachelor’s degree
Posting language: English
Working hours: 40 hours per week
Office presence: 3 days per week

Job summary

The Clinical Trial Coordinator serves as the primary contact for investigative sites, managing site performance, regulatory documentation, and study supply distribution. They are also responsible for processing site invoices, managing payments, and ensuring compliance with study protocols and financial requirements.

Job details

Fortrea's FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal, Canada. Must be bilingual in French & English. Candidates with strong organizational skills, attention to details, and the ability to manage financial processes effectively will be particularly well suited for the role. Job Overview: We are seeking a Clinical Trial Coordinator – Regulatory to serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites. Responsibilities: Serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites. Monitor site performance and implement action plans for sites not meeting expectations, in conjunction with the CRA. Assist CRAs with preparation for site visits (i.e. running reports, QC of files (checking for missing documents), resolving action items from previous visits). Perform Case Report Form review, query generation and resolution against established data review guidelines, under direct supervision on Fortrea or client data management systems, as assigned by management. Assist with the coordination of study visits and shipment of drug, ancillary supplies and laboratory kits/samples. Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines. Liaise with the project team and others to distribute and track clinical trial supplies, e.g. Case Report Forms, study medication, lab kits, ensuring that sites have sufficient supplies to continue recruitment. Proactively work with sites and project teams to ensure maintenance activities (including Amendments, revised documents, etc.) are completed for assigned sites as applicable in region. Demonstrate an understanding of the purpose of CTMS, how to use it, and how to navigate within the different sections. To enter weekly details in CTMS or as per study requirement. Assist in submissions and notifications to Ethics Committees and Regulatory Authorities as applicable in region. Facilitate translation and back translation of all necessary documents as appropriate for local country requirements and as needed regionally. Attend, as needed, meetings (investigator, sponsor, kick-off, face-to-face) and to present at the meetings. Processing site invoices in a timely and accurate manner Managing routine site payments and reimbursements Ensuring payment related activities are completed in accordance with study and financial requirements Collaborating with internal stakeholders to resolve payment inquiries and discrepancies as needed Required to work within SUVODA and COMET/SAP Requirements: At least one year of experience in a related field, (e.g. medical, clinical, pharmaceutical, laboratory research, data analysis, data management or technical writing). 1-2 years of clinical research is required. Basic understanding of biology and biological processes Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP. Good organizational and time management skills Good communication skills, oral and written Exhibits general computer literacy Works efficiently and effectively in a matrix environment Qualifications (Minimum Required): University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology). Fortrea may consider relevant and equivalent experience in lieu of educational requirements. This position is performed through a combination of remote work and in-person at the client's Head Office (2-3 times/week). Physical Demands/Work Environment: General Office Environment. Learn more about our EEO & Accommodations request here.

What you’ll do

Requirements

Candidates must have at least 1-2 years of clinical research experience and a university or college degree in a life science field. Proficiency in both French and English is required, along with a strong understanding of GCP, ICH guidelines, and clinical trial monitoring processes.