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Added 14 mins ago
YO
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Banook

Project Manager - Clinical Trial

Montreal, QC, Canada

💰 Salary: 75–80K CAD · Full-time

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Applications open in a new tab.

Job details

Pay: 💰 Salary: 75–80K CAD
Job type: Full-time
Apply by: Nov 4, 2026
Posting language: English · French
Posted: Oct 5, 2026

Original job description

English section of this bilingual listing.

Banook is a specialized clinical services provider partnering with sponsors and CROs to deliver expert solutions across Cardiac Safety, Central Imaging, Endpoint Adjudication, Functional Respiratory Imaging and eCOA.

We are seeking a Clinical Project Manager to lead complex clinical programs end-to-end, ensuring delivery aligned with GCP, ICH, SOPs, timelines, and financial performance, while driving operational excellence and stakeholder alignment.

👉 Join Banook to contribute to high-impact clinical trials in a rigorous, international, and quality-driven environment.

🔹 Key Responsibilities

Manage end-to-end clinical trial projects (start-up, execution, close-out)
Act as primary sponsor-facing contact and ensure high client satisfaction
Coordinate cross-functional teams (Clinical Data Management, QA, Logistics, Regulatory, Finance)
Ensure compliance with GCP (Good Clinical Practice), ICH guidelines, and SOPs
Develop and maintain Project Management Plans (PMP), risk logs, and study documentation
Monitor KPIs, timelines, deliverables, and performance metrics
Lead risk assessment, issue escalation, and CAPA management
Oversee budgets, forecasting, and financial tracking
Support audits, inspections, and quality assurance activities

🔹 Profile

Bachelor’s or Master’s degree in Life Sciences, Clinical Research, or Healthcare
3+ years’ experience in clinical project management (CRO, pharma, biotech, or service provider)
Strong knowledge of clinical trial lifecycle, GCP, ICH, and regulatory compliance
Experience in multi-study or multi-country trials is a plus
Certification: PMP, PRINCE2, or equivalent (preferred)

🔹 Core Skills

Clinical Project Management • Clinical Trials • Sponsor Management • GCP • ICH • Regulatory Compliance • Risk Management • CAPA • Clinical Operations • Budget Management • Forecasting • KPI Monitoring • Audit Readiness • Cross-functional Leadership • eCOA • EDC • CTMS

🔹 Why Join Banook

High-value positioning as a specialized clinical services provider
Exposure to complex, international clinical programs
Strong culture of quality, ethics, and operational excellence
Collaborative and expert-driven environment
Hybrid work model

🔹 Job Details

📍 Location: Montreal, QC (Hybrid)

💼 Contract: Permanent

💰 Salary: 75–80K CAD

----

Read the full bilingual original

👉 Join Banook to contribute to high-impact clinical trials in a rigorous, international, and quality-driven environment.

🔹 Key Responsibilities

Manage end-to-end clinical trial projects (start-up, execution, close-out)
Act as primary sponsor-facing contact and ensure high client satisfaction
Coordinate cross-functional teams (Clinical Data Management, QA, Logistics, Regulatory, Finance)
Ensure compliance with GCP (Good Clinical Practice), ICH guidelines, and SOPs
Develop and maintain Project Management Plans (PMP), risk logs, and study documentation
Monitor KPIs, timelines, deliverables, and performance metrics
Lead risk assessment, issue escalation, and CAPA management
Oversee budgets, forecasting, and financial tracking
Support audits, inspections, and quality assurance activities

🔹 Profile

Bachelor’s or Master’s degree in Life Sciences, Clinical Research, or Healthcare
3+ years’ experience in clinical project management (CRO, pharma, biotech, or service provider)
Strong knowledge of clinical trial lifecycle, GCP, ICH, and regulatory compliance
Experience in multi-study or multi-country trials is a plus
Certification: PMP, PRINCE2, or equivalent (preferred)

🔹 Core Skills

🔹 Why Join Banook

High-value positioning as a specialized clinical services provider
Exposure to complex, international clinical programs
Strong culture of quality, ethics, and operational excellence
Collaborative and expert-driven environment
Hybrid work model

🔹 Job Details

📍 Location: Montreal, QC (Hybrid)

💼 Contract: Permanent

💰 Salary: 75–80K CAD

----

Banook, est un prestataire spécialisé en services cliniques, partenaire des sponsors et des CRO, apportant une expertise reconnue en Cardiac Safety, Central Imaging, Endpoint Adjudication, Functional Respiratory Imaging et eCOA.

Nous recherchons un(e) Chef de projet en essais cliniques pour piloter des programmes complexes de bout en bout, en garantissant une exécution conforme aux BPC (GCP), aux guidelines ICH, aux SOP, aux délais et aux objectifs financiers, tout en assurant l’excellence opérationnelle et l’alignement des parties prenantes.

👉 Rejoindre Banook, c’est contribuer à des essais cliniques à fort impact dans un environnement international, exigeant et orienté qualité.

Responsabilités principales

Piloter des projets d’essais cliniques de bout en bout (mise en place, conduite, clôture)
Être l’interlocuteur principal des sponsors et garantir leur satisfaction
Coordonner des équipes transverses (Data Management, QA, Logistique, Réglementaire, Finance)
Assurer la conformité aux BPC (GCP), aux guidelines ICH et aux SOP internes
Élaborer et maintenir les plans de management de projet (PMP), analyses de risques et documentation étude
Suivre les KPI, délais, livrables et performance des projets
Piloter la gestion des risques, des écarts et des CAPA
Suivre les budgets, prévisions et aspects financiers des projets
Contribuer aux audits, inspections et activités qualité

Profil recherché

Diplôme en sciences de la vie, recherche clinique ou domaine connexe
Minimum 3 ans d’expérience en gestion de projets cliniques (CRO, pharma, biotech ou prestataire spécialisé)
Bonne maîtrise du cycle de vie des essais cliniques, des BPC/GCP, des guidelines ICH et de la réglementation
Expérience en projets multicentriques ou internationaux appréciée
Certification PMP, PRINCE2 ou équivalent (un atout)

🔹 Pourquoi rejoindre Banook

Positionnement différenciant en tant que prestataire spécialisé
Projets cliniques internationaux et complexes
Culture forte de qualité, d’éthique et d’excellence opérationnelle
Environnement collaboratif et expert
Mode de travail hybride

🔹 Job Details / Informations

📍 Montréal, QC (Hybride)

💼 CDI / Permanent

💰 75–80K CAD

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More about this job

Responsibilities

Lead clinical trial projects from start-up through close-out, serving as the primary sponsor contact and coordinating cross-functional teams. Ensure regulatory and quality compliance while managing project plans, risks, timelines, deliverables, budgets, performance metrics, audits, and corrective actions.

Requirements

Requires a bachelor's or master's degree in life sciences, clinical research, healthcare, or a related field, and at least three years of clinical project management experience. Candidates should know the clinical trial lifecycle, GCP, ICH guidelines, and regulatory compliance; international or multi-country trial experience is an advantage, as is PMP, PRINCE2, or an equivalent certification.

Skills

Clinical Project Management
Clinical Trials
Sponsor Management
Good Clinical Practice
ICH Guidelines
Regulatory Compliance
Risk Management
CAPA Management
Clinical Operations
Budget Management
Forecasting
KPI Monitoring
Audit Readiness
Cross-Functional Leadership
eCOA
EDC

Visa sponsorship

Not detected in the job text

Keywords

Clinical Project Management
Clinical Trials
Clinical Trial Lifecycle
Good Clinical Practice
ICH Guidelines
Standard Operating Procedures
Regulatory Compliance
Project Management Plan
Risk Assessment
Risk Logs
CAPA
Clinical Data Management
Quality Assurance
Regulatory Affairs
Budget Management
Financial Forecasting
KPI Monitoring
Audit Readiness
Sponsor Management
Cross-Functional Teams
Multi-Country Trials
PMP
PRINCE2
eCOA
EDC
CTMS
Cardiac Safety
Central Imaging
Endpoint Adjudication
Functional Respiratory Imaging

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