External Data Acquisition Specialist – Remote

Edupstairs; Mbombela (Nelspruit); A distancia; ZAR 600.000 - 900.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Data Acquisition Specialist to lead the ingestion of External Data Streams for clinical trials. The role involves defining data capture requirements, mapping concepts to the agreed data model and developing Data Transfer Agreements for secure data transfer into the Clinical Data Repository (CDR).

You will collaborate with data stakeholders, ensure regulatory alignment with GCP/ICH guidelines, perform UAT, and monitor data availability across diverse data sources in a remote

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 (Safety Lab, PK, biomarkers, ECG).
• Experience working with external data providers in a clinical study setting.
• Experience developing data transfer agreements.
• Experience working on clinical trials.
• Knowledge of SDTM and data standards.
• Working knowledge of GCP/ICH guidelines.
• Excellent written and verbal communication in English.

Responsabilidades

• Define and set up external data streams as per protocol requirements.
• Coordinate data transfer, ingestion and structure for each data stream.
• Create tsDTA and ensure data transfer frequency aligns with study timelines.
• Liaise with external data providers and internal stakeholders on data requirements.
• Perform UAT of test data transfers and maintain data quality and conformance.

Conocimientos

Excellent English communication

SDTM knowledge

GCP/ICH guidelines

Data transfer agreements

Educación

Bachelor's degree or equivalent (CS preferred)

Descripción del empleo

IQVIA is seeking a Data Acquisition Specialist to lead the ingestion of External Data Streams for clinical trials. The role involves defining data capture requirements, mapping concepts to the agreed data model and developing Data Transfer Agreements for secure data transfer into the Clinical Data Repository (CDR).

You will collaborate with data stakeholders, ensure regulatory alignment with GCP/ICH guidelines, perform UAT, and monitor data availability across diverse data sources in a remote