Key technologies and capabilities for this role
Common questions about this position
Candidates must have 3+ years of data management experience in clinical trials, clinical research, or PMS at pharmaceutical companies, CROs, or academia, along with EDC system build experience, data management team lead experience, and business English usage such as reading SOPs and email communication.
The position is based at the Kamifukuoka office or Osaka office.
Responsibilities include creating input specifications and check specification documents, validating data management systems, performing medical checks and discrepancy checks on case report forms, coordinating with clients and internal departments, and managing dispatched employees.
Yes, experience using English in business contexts, such as reading SOPs and email communication, is required.
The company seeks individuals eager to expand their DM skills, broaden their experience, work globally, and thrive in a challenging environment handling PMS cases, global pharma clinical research, and academia-led investigator-initiated trials.
Advanced analytics and clinical research services
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.