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Band 4 Clinical Trials AdministratorinBirminghaminBirminghamPUBLISHED FRI 13 DEC 2024

Band 4: £26,530 to £29,114 a year  PERMANENT 
NHS

University Hospitals Birmingham NHS Foundation TrustFollow University Hospitals Birmingham NHS Foundation Trust

Opportunity to work in a dynamic and enthusiastic team focused on liver research.
Involvement in a diverse range of studies, including commercial, academic, observational, and complex interventional research.
Development of a wide array of skills, including administration, research systems knowledge, and interpersonal communication.
Experience in liaising with various stakeholders, enhancing professional networking opportunities.
Ability to work independently and manage one's own workload, promoting autonomy and personal responsibility.
Contribution to important research that may improve patient outcomes in liver diseases.
Support and collaboration with experienced research professionals, fostering a learning environment.
The University Hospitals Birmingham NHS Foundation Trust is seeking a Band 4 Clinical Trials Administrator to join their Liver Research Delivery team at Queen Elizabeth Hospital Birmingham. This role involves supporting a diverse range of liver disease studies, including commercial, academic, observational, and interventional research. The successful candidate will assist Research Nurses and the Administration team, while also developing essential skills in administration, research systems, communication, organisation, and documentation.

Key responsibilities include managing research databases, ensuring compliance with data protection and confidentiality policies, collating and transcribing data, checking patient recruitment and consent, and developing IT tracking systems for study documentation. The position requires excellent communication abilities, independent working skills, and strong planning and organisational capabilities to effectively manage a varied workload and collaborate with different stakeholders, including medical professionals, researchers, and external parties.
Opportunity to work in a dynamic and enthusiastic team focused on liver research.
Involvement in a diverse range of studies, including commercial, academic, observational, and complex interventional research.
Development of a wide array of skills, including administration, research systems knowledge, and interpersonal communication.
Experience in liaising with various stakeholders, enhancing professional networking opportunities.
Ability to work independently and manage one's own workload, promoting autonomy and personal responsibility.
Contribution to important research that may improve patient outcomes in liver diseases.
Support and collaboration with experienced research professionals, fostering a learning environment.

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The National Health Service (NHS) is a cornerstone of healthcare in the United Kingdom, established in 1948 with the simple yet profound principle of providing healthcare to all citizens, free at the point of use. This revolutionary system aimed to ensure that access to medical services would not depend on an individual’s financial situation, a concept that has since become fundamental to British societal values.Learn more...
Useful skills for a Band 4 Clinical Trials Administrator:
To work as a Band 4 Clinical Trials Administrator in the UK, you typically need a combination of relevant skills, experience, and qualifications. Here are some key skills and competencies that are often required:
1. Administrative Skills:
- Proficiency in office software (e.g., Microsoft Office Suite: Word, Excel, PowerPoint).
- Strong organizational skills for managing files, documents, and schedules.
- Ability to manage databases and track clinical trial documentation.
2. Communication Skills:
- Excellent written and verbal communication skills to interact effectively with trial participants, healthcare professionals, and regulatory bodies.
- Ability to prepare reports and documentation clearly and accurately.
3. Attention to Detail:
- Strong attention to detail for compliance with protocols and regulations, ensuring that all documents are accurate and complete.
4. Knowledge of Clinical Trials:
- Understanding of clinical trial processes, phases, and regulations (e.g., GCP, ICH guidelines).
- Familiarity with Ethical Review processes and relevant legislation.
5. Interpersonal Skills:
- Ability to work collaboratively in a team environment and interact with a wide range of stakeholders.
6. Problem-Solving Skills:
- Capacity to identify issues, implement solutions, and support the smooth running of clinical trials.
7. Data Management:
- Competence in managing study data, including participant information and trial progress tracking.
8. Regulatory Knowledge:
- Understanding of Good Clinical Practice (GCP) and any other relevant regulatory bodies and their requirements.
9. Time Management:
- Ability to prioritize tasks effectively in a fast-paced environment and meet deadlines.
10. Technical Proficiency:
- Familiarity with data management systems or Clinical Trial Management Systems (CTMS) may be beneficial.
11. Educational Background:
- Relevant qualifications, such as a degree in life sciences, healthcare, or a related field, may be required or preferred.
- A background in research or previous experience in a clinical trial setting can be advantageous.
 


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