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About the Role
The Data Acquisition Specialist defines, sets up, and manages the ingestion of external data streams and related processes to meet clinical trial protocol requirements. This role is crucial for capturing diverse data types from various sources, including central labs, ECG, medical imaging, real-world data, EHR, wearables, and digital technologies, ensuring compliance with data protection laws.
Responsibilities
- Execute deliverables for Standardized External Data Streams.
- Assess external data collection requirements per protocol and plan external data stream set-up activities to meet study start-up timelines.
- Liaise with key data stakeholders to establish data collection purpose and requirements for transfer, ingestion, and structure, ensuring compliance with data protection laws.
- Create change requests for new test concepts or data structures related to external data.
- Develop trial-specific Data Transfer Agreements (tsDTA’s) detailing data transfer, ingestion, and structure requirements.
- Ensure data transfer frequencies meet requirements for medical data review, central monitoring, and reporting.
- Liaise with external data providers to align on and agree tsDTA.
- Translate medical and scientific concepts into data mapping guidance for Clinical Programmers, documented in the annotated Data Transfer Agreement.
- Perform UAT of test data transfers to ensure accuracy and consistency with Data Transfer Agreement specifications.
- Implement data transfer mechanisms for external data streams into CDR, including external provider access.
- Monitor external data stream availability and accuracy, and resolve data transfer issues with external data providers.
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).
- Experience 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.
Experience Level
- Minimum of 3 years’ experience
Education Level
- Bachelor’s degree or equivalent
About the Company
- 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.