Data Acquisition Specialist - External Data (Remote - UK)

IQVIA Argentina; Greater London; Remote; GBP 42,000 - 65,000; Full time

Job summary

IQVIA is seeking a Data Acquisition Specialist to lead the definition, setup and ingestion of External Data Streams aligned with clinical trial requirements. You will coordinate with data stakeholders, create data transfer agreements, and ensure timely data transfer and accuracy across diverse sources including labs, ECG, imaging and real world data.

The role requires a Bachelor’s degree and at least 3 years in clinical data management, strong English communication, and experience with SDTM and

Qualifications

• Bachelor’s degree or equivalent, preferably in Computer Science.
• Minimum of 3 years’ experience managing data in support of clinical research.
• Experience with external data sources (lab, ECG, biomarkers, real world data).
• Experience working with external data providers within a clinical study setting.
• Experience developing data transfer agreements.
• Experience working on clinical trials.
• Experience working in diverse cross-functional, global teams.
• Knowledge of SDTM and working knowledge of GCP/ICH guidelines.
• Excellent written and verbal communication in English.

Responsibilities

• Define, set up and ingest External Data Streams per protocol requirements.
• Collaborate with data stakeholders to define data transfer, ingestion and structure.
• Create change requests for new data concepts or structures.
• Develop trial-specific tsDTA documents detailing data transfer and ingestion.
• Ensure data transfer frequencies meet study needs for review and analysis.
• Liaise with external data providers to align tsDTA agreements.
• Translate medical concepts into data mapping guidance for programmers.
• Perform UAT of test data transfers against Data Transfer Agreements.
• Implement data transfer mechanisms into CDR with external access.
• Monitor data stream availability and resolve transfer issues.

Skills

Data management

Stakeholder liaison

Clinical research

English communication

Education

Bachelor's degree

Tools

SDTM

Job description

The Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture.

External data streams include but are not limited to typical and novel data collected through central labs and ECG, medical imaging, biomarker and genomics analysis, real world data sources, EHR, electronic patient reported outcomes, wearables and sensors and other digital data collection technologies.

Deliverables

• Execute deliverables for Standardized External Data Streams.

• Assess external data collection requirements per protocol and planning of external data stream set-up activities and related deliverables to meet study start-up timelines.

• Liaise with key data stakeholders to establish the purpose of data collection and requirements for the transfer, ingestion, and structure of data for each data stream in compliance with applicable data protection laws and regulations, utilizing available standards and templates

• Create change requests for the definition of new test concepts or data structures relating to external data.

• Develop trial-specific Data Transfer Agreements (tsDTA’s) accurately documenting study requirements and methods for the data transfer, ingestion, and structure.

• Ensure data transfer frequencies are sufficient for the agreed requirements (medical data review, central monitoring, and reporting and analysis).

• Liaise with external data providers to ensure alignment and agreement of tsDTA.

• Translate medical and scientific concepts into data mapping guidance, per agreed data model and documented in the annotated Data Transfer Agreement for use by Clinical programmers.

• UAT of test data transfers ensure accuracy and consistency with data specifications defined in Data Transfer Agreements.

• Implement data transfer mechanisms for external data streams (into CDR) including access for external data providers.

• Monitor availability and accuracy of external data streams, liaise with external data providers to resolve data transfer issues relating to conformance of data.

Education and Experience Requirements

• Bachelor’s degree or equivalent, preferably in Computer Science.

• Minimum of 3 years’ experience managing data in support of clinical research.

• Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG, etc

• Experience in working with external data providers within a clinical study
  setting.

• Experience developing data transfer agreements.

• Experience working on clinical trials.

• Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional.

• Knowledge of SDTM.

• Working knowledge of GCP/ICH guidelines

• Excellent written and verbal communication in English.

This role is not eligible for UK visa sponsorship

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.