Involvement in cutting-edge cancer research and clinical trials, contributing to advancements in medical science and patient care.
Working within one of the largest NHS trusts, which offers significant career development and advancement opportunities.
Collaboration with experienced clinical trial practitioners and research teams, providing valuable mentorship and learning experiences.
Being part of an organization that prioritizes high standards of patient safety and harm-free care, which can enhance job satisfaction.
Engagement in a supportive and inclusive work environment that values diversity and promotes a sense of belonging among staff.
Opportunity to gain practical experience in Good Clinical Practice (GCP) and compliance with national laws and local guidelines.
Job security and benefits associated with working for the NHS, including potential for flexible working arrangements and public sector pensions.
Join Barts Health NHS Trust as a Clinical Trial Assistant in vibrant London and play an integral role in delivering compassionate care through groundbreaking cancer research. As part of the Centre for Experimental Cancer Medicine, you will support a dynamic team dedicated to enhancing clinical trials, ensuring patients receive the highest quality of care. This is an opportunity not just to advance your career, but to make a real difference in the lives of individuals facing cancer, all while working in a nurturing and inclusive environment that celebrates diversity and collaboration.
In this administrative role, you’ll work closely under the guidance of clinical trial practitioners, helping to collect vital clinical data and maintain meticulous records. Your contributions will ensure the smooth operation of our trials and uphold our commitment to excellence and innovation. Embrace a fulfilling career in a pioneering healthcare organisation that values its staff and fosters a sense of belonging, where your dedication truly matters. Ready to take the next step in your journey? For more details or to arrange an informal visit, reach out to Adam Januszewski at adam.januszewski@nhs.net.
In this administrative role, you’ll work closely under the guidance of clinical trial practitioners, helping to collect vital clinical data and maintain meticulous records. Your contributions will ensure the smooth operation of our trials and uphold our commitment to excellence and innovation. Embrace a fulfilling career in a pioneering healthcare organisation that values its staff and fosters a sense of belonging, where your dedication truly matters. Ready to take the next step in your journey? For more details or to arrange an informal visit, reach out to Adam Januszewski at adam.januszewski@nhs.net.
Involvement in cutting-edge cancer research and clinical trials, contributing to advancements in medical science and patient care.
Working within one of the largest NHS trusts, which offers significant career development and advancement opportunities.
Collaboration with experienced clinical trial practitioners and research teams, providing valuable mentorship and learning experiences.
Being part of an organization that prioritizes high standards of patient safety and harm-free care, which can enhance job satisfaction.
Engagement in a supportive and inclusive work environment that values diversity and promotes a sense of belonging among staff.
Opportunity to gain practical experience in Good Clinical Practice (GCP) and compliance with national laws and local guidelines.
Job security and benefits associated with working for the NHS, including potential for flexible working arrangements and public sector pensions.
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:
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More about the NHS
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...
More about CANCER
Cancer remains one of the most significant health challenges in the United Kingdom, impacting millions of lives each year. According to Cancer Research UK, nearly one in two people in the UK will be diagnosed with cancer at some point in their lifetime, highlighting the pervasive nature of this disease.Learn more...
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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