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We're looking for an enthusiastic and dedicated person to join our team in the Directorate of Research & Innovation. You will interpret and record medical research data from clinical trials, completing case report forms and entering data into different research databases. Your responsibilities will include data collection and management for clinical trials and studies across the Trust. You will ensure all work complies with the clinical trial protocol and Good Clinical Practice guidelines, including trials on the NIHR portfolio and commercially funded studies. If you're passionate about research and making a difference to children and young people, we'd love to hear from you!
Job Responsibility:
Interpret and record medical research data from clinical trials, completing case report forms and entering data into different research databases
Ensure the quality and accuracy of data entry, maintaining standards in data integrity
Store and manage data, following the Data Protection Act and relevant guidelines
Update databases to support queries, reporting, and data retrieval
Collaborate with teams, integrating well within the research environment
Apply knowledge of Good Clinical Practice (GCP) and the Research Governance Framework
Develop specialised skills and knowledge in the conduct of clinical trials
Requirements:
Educated to diploma (Level 3) or equivalent level of experience
A good level of IT skills demonstrated by competence in Microsoft software packages i.e. outlook, word processing, database, and spreadsheets
Required to participate in ongoing Professional and Personal Development and undertake additional training as required
Comprehensive administrative/data management experience - preferably in an NHS setting or a busy office environment
Recent project/ research/data collection or clinical audit experience
Data entry experience
Ability to assess, evaluate and interpret clinical/non-clinical information and events against defined protocols in order determine the appropriate course of action
Knowledge of clinical trials
Knowledge of medical terminology
Clear understanding of the importance of confidentiality
Excellent organisational skills
Excellent numerical skills
Excellent communication skills, written and oral
Proven IT skills (including Word, Excel, Access, Outlook)
Problem solving skills
Nice to have:
Evidence of appropriate further education/development
Research qualification
IT Qualification e.g. ECDL Administrative qualifications
Experience of working in an NHS setting/research setting/academic setting
Experience of working within a clinical trial setting
Knowledge of clinical trials data management
Knowledge of research governance and regulations (e.g. ICH-GCP and EU Directives)