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Added 2 mins ago
Appian BPM Technical Lead.
Astra-North Infoteck Inc. ~ Conquering today’s challenges, achieving tomorrow’s vision!
Toronto, ON
Full-time
Design and implement integrations between Appian and enterprise systems (e.g., OnBase, APIs, databases).
Added 2 mins ago
Principal Strategic Deal Maker
Capgemini Engineering
Mississauga, ON
Full-time
Added 2 mins ago
FLIGHT CENTRE - TRAVEL CONSULTANT - NORTH SHORE, BC
Flight Centre Travel Group Canada
BC · British Columbia, Canada
Full-time
This role is rewarding, but it’s not easy, especially in your first few months. You will be learning multiple systems, navigating a wide range of products, and managing high volume customer…
Added 2 mins ago
Machinist II
Motion
North Bay, ON
Full-time
…Install experimental parts or assemblies, such as hydraulic systems, electrical wiring, lubricants or batteries into machines or…
Added 2 mins ago
Maintenance Technician
Trouw Nutrition
Chilliwack, BC
Full-time
Fabricate and install new equipment or systems as required
Added 2 mins ago
Solutions Designer – Senior - RQ11310
S M Software Solutions Inc
Toronto, ON
Internship
…installation, testing, and performance of integrated, multi-service…
Added 2 mins ago
Associate Director
S M Software Solutions Inc
Toronto, ON
Full-time
Lead the evaluation and adoption of agentic AI systems, RAG (Retrieval-Augmented Generation) models, and related technologies to automate repetitive tasks and enhance decision-making.
Added 2 mins ago
Business Analyst – Senior - RQ11684
S M Software Solutions Inc
Toronto, ON
Internship
…Methodology, Enterprise Architecture and Gating Process, and Agile Systems/OPS Standard Systems Development…
Added 2 mins ago
Business Analyst – Senior - RQ11684
S M Software Solutions Inc
Toronto, ON
Internship
…Methodology, Enterprise Architecture and Gating Process, and Agile Systems/OPS Standard Systems Development…
Added 2 mins ago
Associate Director
S M Software Solutions Inc
Toronto, ON
Full-time
Lead the evaluation and adoption of agentic AI systems, RAG (Retrieval-Augmented Generation) models, and related technologies to automate repetitive tasks and enhance decision-making.
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00799
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00798
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00798
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00799
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Software Developer – Senior - RQ11686
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Software Developer with extensive hands-on experience in ServiceNow development, solution architecture, platform governance, and system administration. The…
Added 2 mins ago
Software Developer – Senior - RQ11686
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Software Developer with extensive hands-on experience in ServiceNow development, solution architecture, platform governance, and system administration. The…
Added 2 mins ago
Power Builder Developer - 29954-RFR-DTS-074
S M Software Solutions Inc
Winnipeg, MB
Contract
We are seeking an experienced PowerBuilder Developer to work with one of our Public Sector clients located at 215 Garry Street, Winnipeg, Manitoba. The successful candidate will be…
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00798
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Software Developer – Senior - RQ11686
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Software Developer with extensive hands-on experience in ServiceNow development, solution architecture, platform governance, and system administration. The…
Added 2 mins ago
Associate Director
S M Software Solutions Inc
Toronto, ON
Full-time
Lead the evaluation and adoption of agentic AI systems, RAG (Retrieval-Augmented Generation) models, and related technologies to automate repetitive tasks and enhance decision-making.
Added 2 mins ago
Privacy Impact Assessment (PIA) Specialist – Senior - RQ11603
S M Software Solutions Inc
Toronto, ON
Internship
Added 2 mins ago
Software Developer – Full Stack – Senior - RQ00799
S M Software Solutions Inc
Toronto, ON
Internship
We are seeking a Senior Full Stack Software Developer with extensive experience in enterprise integration, API development, MuleSoft, Apache Camel, Enterprise Java, REST APIs, cloud and…
Added 2 mins ago
Power Builder Developer - 29954-RFR-DTS-074
S M Software Solutions Inc
Winnipeg, MB
Contract
We are seeking an experienced PowerBuilder Developer to work with one of our Public Sector clients located at 215 Garry Street, Winnipeg, Manitoba. The successful candidate will be…
Added 2 mins ago
UX Designer – Senior - RQ11683
S M Software Solutions Inc
Toronto, ON
Internship
Technical Service Blueprint, a diagram that displays the entire process of service delivery including support systems by listing all the activities that happen at each stage, performed by…
Added 2 mins ago
UX Designer – Senior - RQ11683
S M Software Solutions Inc
Toronto, ON
Internship
Technical Service Blueprint, a diagram that displays the entire process of service delivery including support systems by listing all the activities that happen at each stage, performed by…

Fortrea

Clinical Operations Manager (COM) - Montreal, Canada - Hybrid

Montreal, QC, Canada

Job type: Full-time
Apply by: Oct 28, 2026
Posting language: English
Posted: Sep 28, 2026

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Original job description

Fortrea's FSP team is hiring a Clinical Operations Manager 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

Hybrid role in Montreal office 2-3 days per week

Job Overview

Accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight, and impact on local regulatory and financial compliance, at a country operations level at the client. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up. The ability to indirectly influence investigators, vendors, external partners, and country managers to deliver these commitments is a must. This includes adhering to budget targets and agreed payment timelines, addressing and resolving issues, maintaining expertise in country-based regulations, laws and procedures with minimal support from the client management. Requires skilled knowledge of budget and contract negotiations, the local ethics, legislation and regulatory environment, submission and approval processes, development of local Informed Consent as well as other site ready and ongoing study deliverables. Ability to proactively develop risk management and mitigation plans in the country and resolve issues locally.

Summary Of Responsibilities

FINANCIAL (as applicable):
Assistance with the ownership of country and site budgets.
Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.
Oversight and tracking of clinical research-related payments.
Payment reconciliation at study close-out.
COUNTRY SUBMISSIONS and LOCAL LANGUAGE MATERIALS (as applicable):
Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols.
Development of local language materials including local language Informed Consents and translations.
Works in partnership with IRB/IEC and Regulatory Authority in submission and approval related interactions for assigned protocols.
MANAGEMENT and QUALITY OVERSIGHT:
Responsible for managing country deliverables, timelines, and results for assigned protocols to meet country commitments.
Contributes to the development of local SOPs.
COLLABORATION:
Works in close collaboration internally with Clinical country operations (CRD, CRM, CTC, CRA), Country Quality Manager (CQM), Finance, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Business Compliance, Legal and regional operations, Head Quarter functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
Collaborates closely with Regional Operations to align country timelines for assigned protocols. Provides support and oversight to local vendors as applicable.
LOCAL PROCESS OVERSIGHT: (as applicable):
Responsible for clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management.
Enters and updates country information in clinical, regulatory, safety and finance systems.
And all other duties as needed or assigned.

Qualifications (Minimum Required)

University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
In lieu of the above requirement, candidates with a minimum of four (4) or more years of relevant clinical research experience in pharmaceutical or CRO industries or experience in a health care setting will be considered.
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
Thorough understanding of the drug development process
Fluent in local office language and in English, both written and verbal

Experience (Minimum Required)

Good organizational and time management skills.
Working knowledge of ICH, FDA, local regulatory requirements, IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start up documents; previous interaction with operational project team and investigative sites preferred.
Excellent communication skills, oral and written.
Self-motivation with the ability to work under pressure to meet deadlines. Works well independently and in a team environment.
Detail and process oriented.
Positive attitude and approach.
Interact with internal and external customers with a high degree of professionalism and discretion.
Multi-tasking capability.
Good computer skills with good working knowledge of a range of computer packages.
Ability to lead and develop junior staff.
Flexible and adaptable to a developing work environment.
Minimum of four-six (4-6) years of clinical research experience.

Learn more about our EEO & Accommodations request here.

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More about this job

Responsibilities

Oversee country-level clinical trial operations, submissions, approvals, budgets, contracts, payments, timelines, and regulatory compliance. Coordinate with internal teams, sites, vendors, ethics committees, and regulatory authorities to deliver country commitments and manage local processes and risks.

Requirements

Requires a degree or relevant equivalent experience, at least 4–6 years of clinical research experience, and thorough knowledge of ICH, GCP, and applicable regulatory requirements. Candidates must be fluent in French and English and demonstrate strong organization, communication, time management, attention to detail, and the ability to work independently and lead junior staff.

Skills

Clinical Trial Operations
Country Submissions and Approvals
Financial Oversight
ICH Guidelines
Good Clinical Practice
Regulatory Compliance
Informed Consent Development
Risk Management
Project and Timeline Management
Vendor Oversight
Payment Reconciliation
Cross-Functional Collaboration
Local Language Materials
Staff Leadership
Organizational Skills

Visa sponsorship

Not detected in the job text

Keywords

Clinical Operations
Clinical Research
Clinical Trials
ICH Guidelines
Good Clinical Practice
Regulatory Requirements
Country Submissions
Regulatory Approvals
IRB/IEC
Informed Consent
Budget Management
Contract Negotiation
Fair Market Value
Clinical Research Payments
Payment Reconciliation
Risk Management
Standard Operating Procedures
Study Start-Up
Investigator Start-Up Documents
Vendor Management
Site Management
Clinical Trial Agreements
Local Language Translations
Clinical Supplies Management
Import and Export Requirements
Archiving and Retention
Regulatory Compliance
Pharmaceutical Industry
CRO
French and English

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