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
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.
Remote · Canada
Responsible for the execution of clinical trials to meet contractual and regulatory requirements while leading clinical teams. This includes managing project funding, recruitment targets, risk management, and collaborating with stakeholders to accelerate drug commercialization.
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.
Remote · Ottawa, Ontario, Canada
Responsible for monitoring Phase I-IV oncology clinical trials to ensure compliance with protocols and regulatory requirements. Manages site activities from selection and initiation through to close-out and reporting.