Clinical Trial Assistant in London inLondon PUBLISHED THU 10 APR 2025 Jump to job information section
Barts Health NHS Trust rCOpOZd
Job description
This administrative role is essential for the delivery of high quality care in the context of clinical trials. The post-holder will support the smooth running of the Centre for Experimental Cancer Medicine Cancer Research Delivery Group (CECM CRDG) portfolio of clinical trials, contributing to a comprehensive, efficient and effective administration service under the guidance and supervision of research teams and study investigator.
Duties
The post-holder will work under the supervision of clinical trial practitioners and team leads to accurately collect and record essential trial information being mutually supportive and covering duties as necessary during colleagues’ absences and at times of additional pressure, as directed duties will include:
The Barts Health group of NHS hospitals is entering an exciting new era on our improvement journey to becoming an outstanding organisation with a world-class clinical reputation. Having lifted ourselves out of special measures, we now have the impetus and breathing space to chart a fresh course in which we are continually striving to improve all our services for patients.
Our vision is to be a high-performing group of NHS hospitals, renowned for excellence and innovation, and providing safe and compassionate care to our patients in east London and beyond. That means being a provider of excellent patient safety, known for delivering consistently high standards of harm-free care and always caring for patients in the right place at the right time. It also means being an outstanding place to work, in which our WeCare values and behaviours are visible to all and guide us in how we work together.
We strive to live by our WeCare values and are committed to promoting inclusion, where every staff member has a sense of belonging. We value our differences and fully advocate, cultivate and support an inclusive working environment.
For further details / informal visits contact: Name: Adam Januszewski Job title: CRDG Manager Email address:
Duties
The post-holder will work under the supervision of clinical trial practitioners and team leads to accurately collect and record essential trial information being mutually supportive and covering duties as necessary during colleagues’ absences and at times of additional pressure, as directed duties will include:
- Collection of clinical data on Case Report Forms
- Maintenance of a database of trial activity
- Maintaining site files and processing amendments
- Ensuring that the trials are run according to current national law; local guidelines and procedures; following the principles of Good Clinical Practice (GCP)
The Barts Health group of NHS hospitals is entering an exciting new era on our improvement journey to becoming an outstanding organisation with a world-class clinical reputation. Having lifted ourselves out of special measures, we now have the impetus and breathing space to chart a fresh course in which we are continually striving to improve all our services for patients.
Our vision is to be a high-performing group of NHS hospitals, renowned for excellence and innovation, and providing safe and compassionate care to our patients in east London and beyond. That means being a provider of excellent patient safety, known for delivering consistently high standards of harm-free care and always caring for patients in the right place at the right time. It also means being an outstanding place to work, in which our WeCare values and behaviours are visible to all and guide us in how we work together.
We strive to live by our WeCare values and are committed to promoting inclusion, where every staff member has a sense of belonging. We value our differences and fully advocate, cultivate and support an inclusive working environment.
For further details / informal visits contact: Name: Adam Januszewski Job title: CRDG Manager Email address:
Not sure?
If you're interested in this role but you have questions or you're not yet ready to apply, then please book a quick call with us and we'd be happy to answer any questions you have and tell you more about the role.
If you're interested in this role but you have questions or you're not yet ready to apply, then please book a quick call with us and we'd be happy to answer any questions you have and tell you more about the role.
Requirements
See the job description for full role requirements.
Benefits
Benefits are provided by the employer and will be confirmed during your application.
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More information related to this job opportunity, from jobsincare:
Useful skills for a Clinical Trial Assistant:
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To work as a Clinical Trial Assistant (CTA) in the UK, you typically need a combination of education, skills, and experience relevant to clinical research. Here are some key skills and qualifications that are important for this role:
Educational Background
- Relevant Degree: A degree in life sciences, nursing, pharmacy, or a related field is often preferred.
- Knowledge of Clinical Research: Understanding the clinical trial process and Good Clinical Practice (GCP) guidelines.
Key Skills
1. Organizational Skills: Ability to manage multiple tasks, maintain documentation, and ensure trial processes are followed accurately.
2. Attention to Detail: Critical for ensuring that data is recorded correctly and that compliance with regulatory standards is maintained.
3. Communication Skills: Strong verbal and written communication skills to liaise with various stakeholders, including clinical trial personnel, vendors, and regulatory bodies.
4. Technical Skills: Familiarity with database management and clinical trial management systems (CTMS), as well as proficiency with standard office software.
5. Problem-Solving Skills: Ability to anticipate challenges and propose practical solutions.
6. Teamwork and Collaboration: Ability to work effectively within a team, supporting clinical trial staff, such as project managers and clinical research associates.
7. Time Management: Capacity to prioritize tasks and manage time effectively to meet deadlines.
8. Adaptability: Being open to learning and adapting to changes in regulations, protocols, and technology in clinical research.
Experience
- Clinical Research Background: Prior experience in a clinical or research setting, even in an internship or placement, is beneficial.
- Knowledge of Regulatory Requirements: Understanding of British and European clinical trial laws, ethical guidelines, and regulations.
Certifications (optional but beneficial)
- Certifications such as Good Clinical Practice (GCP) can enhance your qualifications and demonstrate your commitment to the field.
Other Considerations
- Networking: Building connections within the clinical research community through events or organizations can provide valuable opportunities and insights.
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51.5072178 -0.1275862 London, England, United Kingdom 
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