Data Acquisition Specialist – External Data

🕒 July 29

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🇬🇧 UK Skilled Worker Visa Sponsor

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👻 Ghost score 33%

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Logo of IQVIA

IQVIA

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.

📋 Description

• Execute deliverables for standardized external data streams • Assess external data collection requirements per protocol and plan stream set-up activities and deliverables to meet study start-up timelines • Liaise with data stakeholders to establish data collection purposes and transfer, ingestion, and structure requirements in compliance with applicable data protection laws and regulations • Create change requests for new test concepts or external-data structures • Develop trial-specific Data Transfer Agreements documenting study requirements and transfer, ingestion, and data-structure methods • Ensure data-transfer frequencies support medical data review, central monitoring, reporting, and analysis • Liaise with external data providers to align on Data Transfer Agreements • Translate medical and scientific concepts into data-mapping guidance for clinical programmers • Conduct UAT of test data transfers for accuracy and consistency with Data Transfer Agreement specifications • Implement external-data transfer mechanisms into CDR, including provider access • Monitor external-data availability and accuracy and resolve transfer conformance issues with providers

🎯 Requirements

• 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 • Experience 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, cross-functional, global, multiregional clinical research teams • Knowledge of SDTM • Working knowledge of GCP/ICH guidelines • Excellent written and verbal communication in English • This role is not eligible for UK visa sponsorship

🏖️ Benefits

• Remote work arrangement in the UK

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