Jobs at IQVIA

Conduct site selection, initiation, monitoring, and close-out visits for clinical trials. Maintain study documentation, support subject recruitment, train sites on protocols, assess site quality, and track regulatory submissions, recruitment, CRF completion, and data query resolution. The role requires collaboration with sites and customers, knowledge of GCP and clinical research regulations, strong organization, and flexibility to travel.

Supports the Records Management department by storing, organizing, retrieving, and managing records and information. Provides records support to employees and departments, accurately processes information, and updates company systems. The role requires strong communication, attention to detail, basic Microsoft Office and database skills, and the ability to manage multiple tasks. Physical duties include extended computer use, accessing stored files, and lifting up to 40 pounds.

Lead complex global oncology clinical studies from initiation through delivery, managing timelines, budgets, risks, stakeholders, sponsors, and cross-functional teams across China, the United States, and Europe. Serve as the primary client contact, support business development, contribute to strategic account growth, and drive project execution in a global matrix organization.

Executes clinical trial site feasibility, identification, activation, regulatory documentation, contracting, and maintenance activities. Serves as the primary contact for investigative sites, prepares and reviews site documents, tracks regulatory and contractual approvals, maintains project systems and timelines, reports site performance metrics, and coordinates with site activation managers, project teams, sponsors, and internal departments.

Drive oncology pharmaceutical sales growth by educating healthcare professionals, managing key accounts, developing territory and market access plans, supporting product adoption, organizing customer events, monitoring competitors, maintaining CRM records, meeting sales targets, reporting adverse events, and complying with pharmaceutical industry standards.

The Consultant, Epidemiologist will support epidemiological study design, perform analyses, conduct literature reviews, and collaborate on projects across APAC, ensuring timely delivery of results.

The role involves building and adapting health economic models, conducting analyses, collaborating with stakeholders, and preparing reports and presentations.

Analyze and support epidemiological studies, perform data analyses, communicate findings, and collaborate with project teams in real world evidence generation.