Remote Data Acquisition Specialist — External Clinical Data

Absa Group

South Africa

Teletrabalho

ZAR 520 000 - 780 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Resumo da oferta

IQVIA is seeking a Data Acquisition Specialist - External Data (Remote/Homebased) to define, set up, and ingest External Data Streams for clinical trials. You will coordinate with labs, imaging, EHR and other data sources, ensuring compliance with data protection laws and established data models.

You will liaise with data stakeholders, draft Data Transfer Agreements, and perform UAT to ensure accuracy of data transfers, contributing to study start-up timelines and global trial delivery.

Qualificações

  • Bachelor's degree or equivalent, preferably in Computer Science.
  • Minimum 3 years' experience managing data for clinical research.
  • Experience with external data sources in clinical studies.
  • Knowledge of SDTM and GCP/ICH guidelines.

Responsabilidades

  • Execute deliverables for Standardized External Data Streams.
  • Assess external data collection requirements per protocol and plan data stream setup.
  • Liaise with data stakeholders to define data transfer, ingestion, and structure per data models.
  • Create change requests for new test concepts or data structures.
  • Develop trial-specific Data Transfer Agreements documenting data transfer needs.

Conhecimentos

Data governance
Clinical data management
Stakeholder communication
Regulatory compliance

Formação académica

Bachelor's degree in Computer Science

Descrição da oferta de emprego

IQVIA is seeking a Data Acquisition Specialist - External Data (Remote/Homebased) to define, set up, and ingest External Data Streams for clinical trials. You will coordinate with labs, imaging, EHR and other data sources, ensuring compliance with data protection laws and established data models.

You will liaise with data stakeholders, draft Data Transfer Agreements, and perform UAT to ensure accuracy of data transfers, contributing to study start-up timelines and global trial delivery.

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