
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
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10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
• Perform activities relating to the definition, set-up and ingestion of External Data Streams • Execute deliverables for Standardized External Data Streams • Assess external data collection requirements per protocol and planning of external data stream set-up activities • Liaise with key data stakeholders to establish the purpose of data collection and requirements for the transfer, ingestion, and structure of data • Create change requests for the definition of new test concepts or data structures relating to external data • Develop trial-specific Data Transfer Agreements (tsDTA’s) • Ensure data transfer frequencies are sufficient for the agreed requirements • Liaise with external data providers to ensure alignment and agreement of tsDTA • Translate medical and scientific concepts into data mapping guidance • UAT of test data transfers ensure accuracy and consistency with data specifications defined in Data Transfer Agreements • Implement data transfer mechanisms for external data streams including access for external data providers • Monitor availability and accuracy of external data streams
• Bachelor’s degree or equivalent, preferably in Computer Science • Minimum of 3 years’ experience managing data in support of clinical research • Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG, etc • Experience in working with external data providers within a clinical study setting • Experience developing data transfer agreements • Experience working on clinical trials • Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional • Knowledge of SDTM • Working knowledge of GCP/ICH guidelines • Excellent written and verbal communication in English
• Health insurance • Retirement plans • Paid time off • Flexible work arrangements • Professional development
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