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 · Canada
Perform site activation, feasibility, and maintenance activities for clinical research studies in accordance with SOPs and regulations. Manage project documentation, track progress, and collaborate with internal teams to ensure site readiness.
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.
Remote · Halifax, Nova Scotia, Canada
The representative acts as a central liaison for patient support programs, managing incoming and outgoing communications with patients and healthcare professionals. They provide clinical support, navigate drug insurance plans, and ensure accurate documentation of patient cases and program logistics.
On-site · Halifax
The Patient Support Specialist acts as a central liaison for patient support programs, providing clinical and administrative assistance to patients, pharmacists, and physicians. They manage reimbursement navigation, handle incoming and outbound communications, and ensure compliance with program quality standards.
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 · 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 · Mississauga
Provide Tier 2 technical and operational support for Veeva applications, including incident resolution and system configuration. Manage client expectations, document solutions, and collaborate with internal teams to ensure system performance and optimization.
Remote · Ottawa, Ontario, Canada
Define the product vision and roadmap for agentic AI initiatives to streamline clinical trial workflows. Lead cross-functional teams to translate business needs into scalable AI solutions while tracking performance metrics.
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.
On-site · Toronto
The Senior Strategic Operations Director leads the governance of assets, resources, and processes for a designated customer portfolio. They act as the primary global contact for operational management, overseeing project teams and ensuring adherence to contractual obligations and strategic business initiatives.
On-site · Laval
The scientist will plan, perform, and document analytical procedures for ligand binding assays, including ELISA, MSD, and Luminex, to evaluate vaccine immunogenicity and efficacy. They will also participate in method development, qualification, and validation phases while maintaining laboratory equipment and inventory.
Remote · Canada
The Senior Safety Project Lead manages service delivery excellence for assigned projects, acting as the primary point of contact for internal and external customers. They are responsible for project planning, financial management, and ensuring compliance with regulatory requirements throughout the product lifecycle.
Remote · Canada
The coordinator supports clinical laboratory projects throughout the study lifecycle by managing daily operations, monitoring performance, and ensuring high-quality deliverables. They also facilitate study start-up, handle protocol-specific documentation, and maintain communication with internal and external stakeholders.
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.
On-site · Montréal
Plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures across international contracts. Manage quality issues, oversee CAPA plans, and provide consultation to project teams and clients regarding regulatory requirements.
On-site · Toronto
The Key Account Manager will drive revenue growth by developing strategic relationships with pharmaceutical clients and managing patient support programs. They will lead cross-functional teams to identify innovative solutions and ensure the successful execution of client program renewals.
On-site · Québec
The Associate Data Analyst performs quantitative and qualitative analyses on healthcare claims data to support internal projects and external client engagements. They are responsible for identifying trends, validating datasets, and producing reports to provide actionable insights for decision-making.
Remote · Canada
The PV Safety Specialist is responsible for managing the collection, reporting, and oversight of safety information in compliance with global and local regulatory requirements. They also support the Local Pharmacovigilance Officer in maintaining safety risk management and ensuring inspection readiness across the affiliate.
On-site · Mississauga
The analyst will conduct quantitative and qualitative research to support client projects in the oncology sector. Responsibilities include interviewing healthcare professionals, analyzing complex datasets, and developing actionable insights for client presentations.
