Jobs for clinical data associate at Montreal

Clinical Data ManagerNexcella, Inc.Greater Montreal / HybridOur 3 Core ValuesIntelligenceIntegrityInitiativeWhat You Will DoDesign eCRF (electronic case report form), review and validation of clinical database.Be responsible for creation of data management plans and other data management documentation as needed with minimal oversight.Support a number of...

Senior CRA (Home-Based) - CanadaICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

Description Location: 600 De Maisonneuve Boulevard West, Montreal, QC H3A 3J2 (100% on-site) Employment Status: Permanent, Full-Time (37.5 hours/week) Schedule: Monday to Friday (must be available to work a schedule that may vary between 6:30 a.m. and 8:00 p.m., depending on operational needs) Please note that there will be approximately three evening...

Description   Location: 600 De Maisonneuve Boulevard West, Montreal, QC H3A 3J2 (100% on-site)Employment Status: Permanent, Full-Time (37.5 hours/week)Schedule: Monday to Friday (must be available to work a schedule that may vary between 6:30 a.m. and 8:00 p.m., depending on operational needs) *Please note that there will be approximately three evening...

Description Location: 600 De Maisonneuve Boulevard West, Montreal, QC H3A 3J2 (100% on-site) Employment Status: Permanent, Full-Time (37.5 hours/week) Schedule: Monday to Friday (must be available to work a schedule that may vary between 6:30 a.m. and 8:00 p.m., depending on operational needs) Please note that there will be approximately three evening...

Description Location: 600 De Maisonneuve Boulevard West, Montreal, QC H3A 3J2 (100% on-site). Employment Status: Permanent, Full-Time (37.5 hours/week). Schedule: Monday to Friday (must be available to work a schedule that may vary between 6:30 a.m. and 8:00 p.m., depending on operational needs). Please note that there will be approximately three evening...

Design eCRF (electronic case report form), review and validation of clinical database.Be responsible for creation of data management plans and other data management documentation as needed with minimal oversight.Support a number of moderate complexity / complex trials with minimal supervision.Monitor progress and conduct of their respective projects,...

As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.What you will be doing:Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

Become a Senior Clinical Associate at IQVIA in Montréal, contributing to the oversight of clinical trials and ensuring compliance with regulations. Bilingualism in French and English is essential. The ideal candidate has a strong background in site management and at least three years of monitoring experience. Your responsibilities will include conducting...

Senior Lead Clinical Data Manager (Equivalent to project lead DM) Remote – US / Canada The Company: Join a Top 5 Global CRO at the forefront of data science in clinical trials. You’ll collaborate directly with leading pharma sponsors, gain exposure to diverse therapeutic areas, and shape your career in a true leadership role. What You’ll Do: Act as...

Une entreprise de recherche clinique de premier plan recherche un professionnel à Montréal pour effectuer des tâches de suivi et de gestion de site selon les protocoles cliniques. Le candidat doit avoir un baccalauréat en science ou soins de santé et 3 ans d'expérience en surveillance de site. Les compétences en communication et la maîtrise de...

Nexcella, Inc. is seeking an Associate Director of Regulatory Affairs to guide regulatory strategy and execution for clinical trials under FDA/EMA/Health Canada/MHRA regimes.The role focuses on preparing, submitting, and maintaining regulatory documents to ensure compliance with applicable laws, with attention to detail and strong analytical skills. Ideal...

The University of Ottawa Heart Institute Research Corporation is seeking a Research Assistant to support innovative clinical research focused on improving patient health outcomes. Working under the direction of the Principal Investigator, Research Manager, and Research Coordinator, the Research Assistant will play an important role in participant...

ResponsibilitiesDesign, govern and evolve health data interoperability modelsTranslating clinical and operational needs into standardized and semantically consistent data modelsDefine and maintain FHIR profiles, implementation guides, and conceptual and logical data modelsAlign solutions with recognized interoperability standards, including HL7 FHIR, HL7 v2,...

​​​​​​​​​​​​​​​​​​​​​​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...

Export Development Canada (EDC) is hiring an Associate Data Platform Administrator in Ottawa. The role focuses on supporting data and analytics platforms, with hands-on tasks in cloud-based environments and a path to grow in data platform engineering. Ideal candidates have 2+ years in IT, ITSM exposure, and familiarity with Azure DevOps, CI/CD, and Git. The...

Please refer to the How to Apply for a Job (for External Candidates) job aid for instructions on how to apply.If you are an active McGill employee (ie: currently in an active contract or position at McGill University), do not apply through this Career Site. Login to your McGill Workday account and apply to this posting using the Find Jobs report (type Find...

​​​​​​​​​​​​​​​​​​​​​​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...

​​​​​​​​​​​​​​​​​​​​​​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...

Company DescriptionPSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.Job Description Coordinates investigator/ site feasibility and...