Remote External Data Acquisition Specialist (Clinical Trials)

Placements24

Upington

Remote

ZAR 420.000 - 700.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

IQVIA seeks a Data Acquisition Specialist - External Data (Remote/Homebased) to define, set up and ingest external data streams for clinical trials, ensuring data quality and compliance.

You will collaborate with data stakeholders, develop data transfer agreements, and perform UAT on data transfers, supporting study start-up timelines and cross-functional data projects. Strong SDTM knowledge and English communication are essential, with 3+ years in clinical data management.

Qualifikationen

  • Bachelor's degree or equivalent (preferably in Computer Science)
  • Minimum 3 years' experience managing data in clinical research
  • Experience with external data sources in clinical trials
  • Experience working with external data providers in a clinical study setting
  • Knowledge of SDTM and GCP/ICH guidelines
  • Excellent written and verbal communication in English

Aufgaben

  • Define the setup and ingestion of External Data Streams per protocol
  • Coordinate data transfer, ingestion and structure with stakeholders
  • Create change requests for data concepts or structures
  • Develop trial-specific Data Transfer Agreements documenting requirements
  • Ensure data transfer frequencies meet study timelines
  • Perform UAT of test data transfers for accuracy
  • Implement data transfer mechanisms for external data streams into CDR
  • Monitor availability and quality of external data streams and resolve issues

Kenntnisse

Data management
English communication

Ausbildung

Bachelor's degree or equivalent

Jobbeschreibung

IQVIA seeks a Data Acquisition Specialist - External Data (Remote/Homebased) to define, set up and ingest external data streams for clinical trials, ensuring data quality and compliance.

You will collaborate with data stakeholders, develop data transfer agreements, and perform UAT on data transfers, supporting study start-up timelines and cross-functional data projects. Strong SDTM knowledge and English communication are essential, with 3+ years in clinical data management.

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