Senior Data Acquisition Specialist – External Clinical Data

VKB Agriculture; South Africa; A distancia; ZAR 650.000 - 900.000; Jornada completa

Descripción de la vacante

IQVIA seeks a Data Acquisition Specialist - External Data (Remote/Homebased) to manage and implement standardized external data streams across multiple global studies. You will liaise with data providers, draft tsDTA agreements, and ensure compliant data transfer, ingestion, and structure for study start-up timelines.

You will collaborate with stakeholders to translate data concepts into actionable mapping guidance for Clinical programmers, perform UAT, and monitor data availability and quality

Formación

• Bachelor's degree or equivalent; preferably in Computer Science.
• Minimum of 3 years' data management experience in clinical research.
• Experience with external data providers in a clinical study setting.
• Knowledge of SDTM.
• Working knowledge of GCP/ICH guidelines.
• Excellent written and verbal communication in English.

Responsabilidades

• Execute deliverables for standardized external data streams.
• Assess external data collection requirements and plan data stream setup.
• Coordinate with data stakeholders on data transfer and structure per regulations.
• Create change requests for new test concepts or data structures.
• Develop trial-specific data transfer agreements documenting requirements.
• Ensure data transfer frequencies meet study needs (review, monitoring, reporting).
• Coordinate with external data providers on tsDTA alignment.
• Translate concepts into data mapping guidance for Clinical programmers.
• Perform UAT of test data transfers for data specification conformance.
• Implement data transfer mechanisms into CDR and provide external access.
• Monitor data stream availability and resolve transfer issues with providers.

Conocimientos

Communication in English

Educación

Bachelor's degree or equivalent (prefer Computer Science)

Descripción del empleo

IQVIA seeks a Data Acquisition Specialist - External Data (Remote/Homebased) to manage and implement standardized external data streams across multiple global studies. You will liaise with data providers, draft tsDTA agreements, and ensure compliant data transfer, ingestion, and structure for study start-up timelines.

You will collaborate with stakeholders to translate data concepts into actionable mapping guidance for Clinical programmers, perform UAT, and monitor data availability and quality