Remote Data Acquisition Specialist – Clinical Trials

Nhs Ayrshire & Arran

South Africa

A distancia

ZAR 420.000 - 640.000

Jornada completa

Hace 9 días

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Descripción de la vacante

IQVIA in South Africa is seeking a Data Acquisition Specialist - External Data (Remote/Homebased). You will define, set up and ingest External Data Streams for clinical trials, ensuring data transfer, ingestion and structure align with protocol requirements and data protection laws.

You will liaise with data stakeholders, coordinate with external data providers and perform UAT, data mapping guidance, and documentation including tsDTA, with a focus on data quality and timely study startup

Formación

  • Bachelor's degree or equivalent, preferably in Computer Science.
  • Minimum of 3 years' experience managing data in clinical research.
  • Experience with external data sources (labs, ECG, imaging, EHR, wearables).
  • Experience developing data transfer agreements.
  • Experience working on clinical trials in diverse, multi-regional teams.
  • Knowledge of SDTM and GCP/ICH guidelines.
  • Excellent written and verbal English communication.

Responsabilidades

  • Execute deliverables for standardized external data streams.
  • Assess external data collection requirements per protocol and plan set-up activities.
  • Liaise with data stakeholders to define data collection purpose and transfer/ingestion requirements.
  • Translate concepts into data mapping guidance and document in annotated DTA.
  • Perform UAT of test data transfers for accuracy with data specs.
  • Ensure data transfer mechanisms for external data streams into CDR.

Conocimientos

Data management
Clinical research coordination
External data handling
Data transfer agreements
SDTM knowledge
GCP/ICH knowledge
English communication

Educación

Bachelor's degree in Computer Science or related field

Descripción del empleo

IQVIA in South Africa is seeking a Data Acquisition Specialist - External Data (Remote/Homebased). You will define, set up and ingest External Data Streams for clinical trials, ensuring data transfer, ingestion and structure align with protocol requirements and data protection laws.

You will liaise with data stakeholders, coordinate with external data providers and perform UAT, data mapping guidance, and documentation including tsDTA, with a focus on data quality and timely study startup

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