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.
On-site · Mississauga
The statistical programmer is responsible for analyzing project requirements, executing programming tasks using SAS and SQL, and ensuring client expectations are met. They must also perform thorough quality assurance, maintain code, and produce timely project deliverables.
Hybrid · Mississauga
The consultant will provide strategic consulting support to life sciences clients by analyzing business challenges and developing evidence-based solutions. They will collaborate with cross-functional teams to deliver high-quality projects related to market access, health economics, and product access strategies.
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.
On-site · Québec
The Financial Analyst provides analytical support and financial insights for management reporting, budgeting, and forecasting. They are responsible for reconciling data across systems and identifying drivers of financial variances.
On-site · Kirkland
Design and update electronic case report forms, edit specifications, and EDC system components for clinical studies, while coordinating design reviews and collaborating with study stakeholders. Manage multiple study design projects, monitor timelines, budgets, risks, and quality, and contribute to process improvements.
Remote · Canada
The Site Activation Specialist manages site feasibility, regulatory documentation, and contract negotiations for clinical research projects. They serve as the primary point of contact for investigative sites and ensure all project timelines and SOP requirements are met.
Remote · Toronto, Ontario, Canada
Conduct independent, standardized psychiatric assessments of patients for a major depressive disorder clinical study. Administer, score, review, or oversee MADRS and MINI assessments to support the quality and integrity of clinical trial outcomes.
On-site · Mississauga
Conduct statistical programming for clinical data using SAS while ensuring compliance with ICH guidelines and company SOPs. Generate analysis datasets according to CDISC standards and assist in the preparation and review of SAP and TLF shells.
Hybrid · Mississauga
The analyst will assist in reviewing client requirements and performing quantitative or qualitative analysis to develop tailored solutions. They will also contribute to the creation of detailed documentation and presentations under the supervision of senior team members.
On-site · Kirkland
The Senior Customer Success Associate manages project documentation, quality control, and data validation to ensure accurate and timely delivery of measurement projects. They also serve as a primary point of contact for clients, providing strategic insights and mentoring junior team members.
On-site · Kirkland
Lead end-to-end UX research and design initiatives for AI-enabled clinical technology solutions within the Applied Data Science Center. Collaborate with multidisciplinary teams to translate complex clinical and AI-assisted workflows into intuitive, scalable digital experiences.
On-site · Kirkland
The Senior Customer Success Associate manages project documentation, quality control, and data validation to ensure accurate and timely delivery of measurement projects. They also serve as a primary point of contact for clients, providing strategic insights and mentoring junior team members.
Remote · Canada
The specialist manages site activation activities, including feasibility assessments, regulatory documentation, and site identification. They also negotiate contracts and budgets while serving as the primary point of contact for investigative sites.
Remote · Canada
Direct and manage the strategic, operational, and financial execution of site activation activities, including site selection, regulatory processes, and contract negotiations. Collaborate with internal and external stakeholders to ensure project timelines and quality standards are met throughout the clinical study lifecycle.
On-site · Québec
The Associate Manager will support the lifecycle management of COA products, including development, commercialization, and delivery of licenses. They will also collaborate with internal teams to define deliverables, manage client expectations, and support business development initiatives.
On-site · Québec
The Business Development Analyst will identify and qualify new business opportunities within the Canadian healthcare sector while managing client relationships. They are responsible for coordinating pursuit activities, maintaining the CRM pipeline, and supporting strategic growth initiatives across Canada.
On-site · Mississauga
The Senior Consultant leads scientific and pricing assessments for pharmaceutical clients, managing project workstreams and providing evidence-based strategic recommendations. They also act as a primary client contact, mentor junior team members, and ensure all deliverables meet high quality and regulatory standards.
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 Clinical Independent Rater ensures the integrity of clinical trial data by reviewing assessment quality and providing guidance to raters. Responsibilities include conducting live interactions with raters to provide feedback on methodology and scoring techniques.
