IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences, enhancing healthcare outcomes through intelligent data connections.
Durham, North Carolina
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Remote · Ottawa, Ontario, Canada
Monitor Phase I–IV oncology clinical trials and manage site activities from start-up through close-out, ensuring compliance with study protocols, GCP/ICH guidelines, and regulatory requirements. Train site personnel, oversee documentation and investigational product accountability, resolve data queries, maintain site communications, and prepare monitoring reports.
On-site · Mississauga
Perform site monitoring visits and manage site activities for various clinical protocols in compliance with GCP and ICH guidelines. Ensure data integrity, manage regulatory submissions, and support subject recruitment plans while maintaining effective communication with study sites.
On-site · Kirkland
Perform site monitoring visits and manage site activities for various clinical protocols to ensure regulatory compliance and data integrity. Collaborate with study teams to drive subject recruitment and maintain essential study documentation according to GCP/ICH guidelines.
On-site · Kirkland
The Clinical Research Associate will monitor and manage clinical trial sites to ensure compliance with protocols, regulations, and sponsor requirements. They are responsible for conducting site visits, overseeing subject recruitment, and maintaining accurate study documentation.
On-site · Kirkland
Monitor and manage clinical trial sites to ensure studies are conducted in accordance with protocols, regulations, and sponsor requirements. Conduct site visits, manage recruitment plans, and maintain essential study documentation to ensure data integrity and compliance.
On-site · Kirkland
Rejoignez une équipe qui fait progresser la recherche clinique Nous recherchons un(e) associé(e) de recherche clinique (CRA) passionné(e) et motivé(e) pour rejoindre notre équipe et jouer un rôle clé dans la réalisation d’essais cliniques de haute qualité. Dans ce rôle, vous collaborerez avec les sites investigateurs et les équipes transversales afin de garantir que les études sont menées avec excellence, conformité et centrées sur les patients. Aperçu du poste Surveiller et gérer les centres pour s’assurer qu’ils réalisent les études et produisent des rapports sur les données d’étude con…
On-site · Kirkland
The Clinical Trial Manager is responsible for the successful execution of clinical trials by managing project requirements, timelines, and clinical teams. They ensure compliance with regulatory standards, manage project risks, and oversee clinical budgets and stakeholder communication.
On-site · Québec
The Clinical Trial Educator provides training on trial criteria to healthcare providers and coordinators to improve patient recruitment. They also collaborate with clinical research associates and referring physicians to develop recruitment plans and support trial execution.
Remote · Ottawa, Ontario, Canada
The Clinical Research Associate II is responsible for monitoring Phase I–IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. They manage site activities from start-up through close-out, including site visits, training, and documentation quality assurance.
Remote · Canada
The role involves managing client relationships and project delivery for connected devices within clinical research. Responsibilities include developing departmental strategy, overseeing quality control, and ensuring compliance with regulatory guidelines.
Remote · Canada
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
On-site
French Job Description- Niveau du poste : Spécialiste des opérations d’essais cliniques Lieu : Télétravail au Canada (à domicile) Aperçu du poste: Fournir un soutien opérationnel et une coordination pour les essais cliniques internationaux, en veillant à leur bon déroulement, de la planification à la clôture. Gérer la documentation, les systèmes, la communication et la logistique liés aux essais, conformément aux procédures opérationnelles normalisées (SOP), aux BPC-ICH et aux exigences réglementaires, tout en respectant les objectifs de qualité et de délais. Fonctions essentielles: Planifier…
On-site · Kirkland
The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.
On-site · Mississauga
The role involves performing monitoring and site management tasks across various protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing subject recruitment plans, administering study training, evaluating site quality and integrity, and ensuring proper documentation in the Trial Master File and Investigator's Site File.
On-site · Kirkland
Perform site monitoring visits to ensure study conduct adheres to protocols, regulatory requirements, and GCP/ICH guidelines. Manage site progress by tracking regulatory submissions, subject recruitment, and data integrity while maintaining essential study documentation.
On-site · Kirkland
The Senior Clinical Research Associate performs site monitoring visits, including selection, initiation, and close-out, to ensure compliance with GCP and ICH guidelines. They also manage site recruitment plans, oversee regulatory submissions, and maintain essential study documentation.
On-site · Kirkland
Chef principal des essais cliniques IQVIA Biotech collabore exclusivement avec des entreprises de biotechnologie et des sociétés biopharmaceutiques émergentes pour soutenir le développement clinique à toutes les phases et dans tous les domaines thérapeutiques. Notre structure agile, notre culture collaborative et notre expertise thérapeutique approfondie nous permettent d'offrir des solutions sur mesure qui contribuent à accélérer l'accès des patients à des traitements innovants. IQVIA Biotech est à la recherche d'un(e) Chef principal des essais cliniques possédant de l'expérience en onco…