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# Data Officer (Internal)

- **Company:** Cardiff and Vale University Health Board
- **Location:** Hereford, UK
- **Salary:** £28,392.0 - £31,157.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Software Applications, Microsoft Outlook, Spreadsheets, Clinical Data Repository, Databases, Data Validation, Microsoft Office, Microsoft PowerPoint, Google Cloud, Computerised Systems
- **Published:** October 31, 2026
- **Apply:** https://www.jobs.nhs.uk/candidate/jobadvert/C9229-26-0965/ats-direct-apply

## About the Role

* Level 3 qualification in Administration or equivilant experience and knowledge relevant to clinical data or research
 * Good standard of education to minimum GCSE English and Maths A-C/4-9 or equivalent
 * ICH GCP Training Certificate or willingness to undertake, * Knowledge and understanding of relevant legislation and guidelines (e.g. GCP, GDPR, Research Governance Framework)
 * Good working knowledge of medical terminology, preferably clinical trials specific
 * Familiarity with NHS clinical and information processes and systems
 * Advanced IT skills with ability to work simultaneously across multiple computer applications
 * Ability to interpret and abstract complex information summarising and reporting various forms of data
 * Excellent attention to detail, methodical with high standards of accuracy
 * Ability to deal with sensitive and confidential information
 * Excellent written and verbal communication skills
 * Excellent interpersonal skills in order to work effectively with a wide range of health professionals and as part of a team
 * Well developed analytical and problem solving skills
 * Well organised and skilled in time management with ability to meet deadlines and also work with several projects simultaneously, * Experience in a NHS clinical administrative role
 * Working knowledge of Trust computerised systems
 * Expert user of Microsoft office programmes e.g. Excel, PowerPoint, Word, Outlook
 * Highly IT competent with experience using clinical databases (e.g. EDGE, REDCap, or similar)
 * Experience of basic data management processes, * Prior experience in a clinical research environment
 * Project management experience, * Professional and flexible approach
 * Commitment to high standards and continuous improvement
 * Ability to work independently and as part of a team
 * Mental effort- Frequent requirement for intense concentration Positive, proactive attitude to learning and development

Other factors

## Description

*Internal Applicants Only*

We are seeking an enthusiastic and organised individual with experience of working in a clinical environment to join our Clinical Trials Team. The post holder will coordinate data collection, entry, validation and reporting across a range of clinical studies and specialties, ensuring data is accurate, complete and submitted within deadlines.

Working independently, the successful candidate will liaise with clinical and research teams, Principal Investigators, sponsors and Clinical Trials Units to resolve data queries, coordinate patient assessments and follow-ups, maintain trial documentation and ensure compliance with study protocols, Good Clinical Practice (GCP), research governance and data protection requirements., * Collect, enter, validate and report clinical trial data accurately and within deadlines.

 * Identify and resolve data discrepancies, respond to queries and escalate concerns appropriately.
 * Coordinate patient assessments, appointments, recruitment and follow-up activities in line with trial protocols.
 * Liaise with clinical teams, researchers, sponsors and Clinical Trials Units.
 * Maintain trial records, site files, spreadsheets, databases and EDGE recruitment reports.
 * Ensure compliance with research protocols, GCP, governance requirements and patient confidentiality.
 * Undertake data quality checks, internal audits and support audit readiness.
 * Review and improve data collection processes, SOPs and work instructions.
 * Provide guidance and training to colleagues on clinical trial data procedures.
 * Manage competing priorities, contribute to research promotion and service improvement., The full job description provides an overview of the key tasks and responsibilities of the role and the person specification outlines the qualifications, skills, experience and knowledge required.