ich jobs in Montreal

Nous sommes présentement à la recherche d’un·e Chef·fe d’équipe – Contrôle Qualité pour un poste permanent à temps plein.La personne titulaire de ce poste sera appelée à participer à la planification et au suivi des activités liées au contrôle de la qualité ainsi qu’à la gestion du programme de stabilité. Elle pourra également être...

Translational Research in Oncology (TRIO)is a global academic clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource...

Translational Research in Oncology (TRIO)is a global academic clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource...

Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resources team....

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...

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...

Rejoignez l'équipe à Montréal, Québec, en tant que Responsable Assurance Qualité et Réglementaire. Ce rôle hybride se concentre sur la gestion de la qualité et la conformité réglementaire. Nous recherchons un expert en QA/RA avec 4 à 6 ans d'expérience dans une CRO ou une entreprise pharmaceutique. Vous serez responsable de déployer et...

Lead clinical protocol and regulatory writing for dicentra from Ontario, working fully remotely across clinical research projects. Translate complex scientific data into compliant documents.As a Senior Medical and Regulatory Writer, you will support pharmaceuticals, medical devices, and natural health products. You will independently manage complex...

The Research Institute of the MUHC (RI-MUHC) in Montreal seeks a Clinical Trial Project Manager to oversee multicentre studies, regulatory submissions, and operational study management. You will coordinate start-up, site activations, monitoring, data integrity, and safety reporting across MUHC and external sites, ensuring adherence to protocol and...

ICON plc in Montreal is seeking a Senior Clinical Research Associate (CRA) fluent in French and English to monitor clinical studies at sites or remotely, ensuring compliance with protocol, SOPs, ICH-GCP, and regulatory requirements.The role requires a Bachelor's degree in a health-related field, 1+ years monitoring experience (3+ for higher levels), oncology...

Indero, a CRO specializing in dermatology and rheumatology, seeks a Project Director to oversee a portfolio of global trials and lead Project Managers across studies in multiple regions from startup to closure.You will contribute to proposal development, ensure adherence to GCP/ICH and regulatory standards, and drive operational efficiency and strategic...

Principal Medical WriterThe Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

dicentra Inc. is seeking an experienced Clinical Trial Manager to oversee active programs, site operations, and monitoring activities. The role can be full-time, part-time fixed-term, or independent consulting, depending on experience.You will own operational delivery for studies across phases, ensure ICH-GCP compliance, and coordinate with data management...

ICON plc is seeking a Senior Clinical Research Associate (CRA) to monitor clinical studies from home across Canada. You will ensure trials are conducted, documented and reported in accordance with the protocol, SOPs, ICH-GCP and applicable regulations.The role requires a Bachelor’s degree in a scientific/health field and 1+ years of monitoring experience;...

St-Amour is seeking a Project Manager to lead cross-functional pharmaceutical initiatives aimed at operational excellence and regulatory compliance. You will work with Quality, Regulatory Affairs, R&D, Supply Chain, Finance and Commercial Operations to ensure projects meet timelines and budgets.You will develop project charters, monitor KPIs, and drive...

Alimentiv is seeking a TMF Coordinator to maintain quality and compliance of Trial Master File documentation, ensuring inspection readiness and alignment with ICH-GCP and FDA/EMA expectations. You will file, index, and manage TMF content across eTMF systems like Veeva Vault, Phlexglobal, and Trial Interactive, while collaborating with study teams and QA to...

TRIO - Translational Research in Oncology in Canada is seeking a Clinical Research Associate to join the Monitoring Resources team. This remote position supports Western Canada (BC/AB/SK/MB) and reports to the CRA Line Manager. The role involves site visits, regulatory compliance, data verification, and collaboration across teams.You will work independently...

MiRus is seeking a Clinical Research Associate to support cardiovascular medical device studies, focusing on timelines, data integrity, and high-quality documentation.The role requires a clinical nursing background with cardiac experience and familiarity with FDA/ICH/GCP guidelines, plus CRA certification is preferred. Travel may be required while...

TRIO - Translational Research in Oncology is seeking a Clinical Research Associate to join our Monitoring Resource team. This remote, full-time freelance opportunity is a 1-year contract open to candidates in Western Canada (BC, AB, SK, MB).Responsibilities include site visits, data verification, and ensuring FDA/ICH-GCP compliance while mentoring junior...

AbCellera is seeking a Clinical Project Manager to serve as the Regional Lead and tactical owner of study execution in the assigned countries. You will lead a cross-functional team to deliver on our clinical trials while maximizing our footprint across regional health networks and trial sites.You will drive global strategy at the site level, mentor...