Remote Data Acquisition Specialist - External Data

Meeveem Limited; United Kingdom; Remote; GBP 45,000 - 65,000; Full time

Job summary

IQVIA is seeking a Data Acquisition Specialist for External Data (Remote - UK). You will manage external data streams, define data transfer protocols, and collaborate with data stakeholders to ensure compliant ingestion for clinical trials. The role requires SDTM knowledge and strong English communication.

Join a global leader in clinical research services and work in a cross‑functional, multi‑regional team to support study start‑up timelines and data quality.

Qualifications

• Bachelor's degree in Computer Science or equivalent.
• Minimum 3 years' experience managing data in clinical research.
• Experience with external data sources (ECG, PK, biomarkers).
• Experience developing data transfer agreements.
• Knowledge of SDTM and GCP/ICH guidelines.
• Excellent written and verbal English communication.

Responsibilities

• Execute deliverables for Standardized External Data Streams.
• Plan external data set-up aligned with protocol timelines.
• Liaise with data stakeholders to define data transfer and structure per data models.
• Create change requests for new test concepts or data structures.
• Develop trial-specific tsDTA documenting data transfer requirements.
• Ensure data transfer frequencies meet study requirements.
• Coordinate with external data providers to align on tsDTA.
• Translate medical concepts into data mapping guidance.
• UAT of test data transfers against Data Transfer Agreements.
• Monitor availability and accuracy of external data streams.

Skills

Data management

SDTM

GCP/ICH

Data mapping

Cross-functional teamwork

English communication

Education

Bachelor's degree (CS preferred)

Job description

IQVIA is seeking a Data Acquisition Specialist for External Data (Remote - UK). You will manage external data streams, define data transfer protocols, and collaborate with data stakeholders to ensure compliant ingestion for clinical trials. The role requires SDTM knowledge and strong English communication.

Join a global leader in clinical research services and work in a cross‑functional, multi‑regional team to support study start‑up timelines and data quality.