Clinical Trials AssistantinSheffieldinSheffieldPUBLISHED TUE 14 JAN 2025
Opportunity to work in a leading NHS organization known for research excellence, enhancing professional credibility.
Involvement in a diverse range of clinical trials, providing a rich experience in various areas of medical research.
Ability to support and directly engage with research participants, making a tangible impact on patient care and outcomes.
Access to professional development opportunities and training, fostering career growth and skill enhancement.
Work collaboratively with a multi-disciplinary team, promoting a supportive and engaging work environment.
Flexibility offered through a fixed-term contract with the possibility of extension, accommodating personal circumstances.
Strong emphasis on work-life balance supported by various employee policies, enhancing overall job satisfaction.
The Clinical Trials Assistant (CTA) role at Sheffield Teaching Hospitals NHS Foundation Trust involves supporting the delivery of clinical research and managing a range of research studies within the NHS environment. The post holder will assist in all aspects of clinical trial operations, from study setup to data archiving, working in compliance with clinical trial protocols and regulatory standards. Duties include document submission to the Clinical Research and Innovation Office (CRIO), data collection and maintenance, providing administrative support to research staff, conducting clinical tests, and facilitating participant screening and recruitment.
This position is a fixed-term contract, lasting up to twelve months due to maternity leave, and offers opportunities for professional development in a supportive and respected environment. The CTA Team collaborates across various sites and is instrumental in conducting studies under the NIHR Sheffield Biomedical Research Centre and Clinical Research Facility. Candidates interested in the role can contact Nicola Tinker for further discussion about the job description and requirements.
This position is a fixed-term contract, lasting up to twelve months due to maternity leave, and offers opportunities for professional development in a supportive and respected environment. The CTA Team collaborates across various sites and is instrumental in conducting studies under the NIHR Sheffield Biomedical Research Centre and Clinical Research Facility. Candidates interested in the role can contact Nicola Tinker for further discussion about the job description and requirements.
Opportunity to work in a leading NHS organization known for research excellence, enhancing professional credibility.
Involvement in a diverse range of clinical trials, providing a rich experience in various areas of medical research.
Ability to support and directly engage with research participants, making a tangible impact on patient care and outcomes.
Access to professional development opportunities and training, fostering career growth and skill enhancement.
Work collaboratively with a multi-disciplinary team, promoting a supportive and engaging work environment.
Flexibility offered through a fixed-term contract with the possibility of extension, accommodating personal circumstances.
Strong emphasis on work-life balance supported by various employee policies, enhancing overall job satisfaction.
If you are interested in this post, and would like to discuss the job description, person specification or job role, please contact Nicola Tinker who will be happy to discuss this with you.
The post holder will join the Clinical Trials Assistant (CTA) Team, with one of the Directorate Research Teams. The CTA Team work cross-site, to support the delivery of first class quality care to research participants within Sheffield Teaching Hospitals NHS Foundation Trust (STH). The CTA Team manage a portfolio of research studies that are conducted within STH Clinical Directorates and within the NIHR Sheffield Clinical Research Facility (CRF).
The post holder will assist in supporting a portfolio of clinical trials, from study set up to archiving, in accordance with clinical trial protocols, laboratory manuals and all relevant regulatory standards.
The role will involve completing and submitting documents to the Clinical Research and Innovation Office (CRIO) obtain approvals; collecting, recording and maintaining research data records; entering activity data and extracting information from databases, providing clinical and administrative support to Research Nurses including performing clinical tests and investigations, processing and shipping samples and assisting with screening and recruitment processes. Post holders may also support, and be responsible for, relevant studies in their own right.
You will be working for an organisation which values and respects all of its staff and the community it serves. The Trust is a leader in the NHS and research sectors and provides excellent benefits for its staff. This includes commitments to professional development but also many policies to support employees in balancing their personal and professional lives.
The CTA Team is part of the Clinical Research and Innovation Office (CRIO), and one of the Directorate Research Teams. It is involved in the delivery of clinical research across STH. We support the delivery of a wide range of studies, including studies from within the NIHR Sheffield Biomedical Research Centre (BRC) and NIHR Sheffield Clinical Research Facility (CRF).
This vacancy is advertised on a fixed term contract basis for a period of a maximum of twelve months due to maternity leave of the substantive post holder. The fixed term contract status of the post holder will be reviewed in accordance with the Trust's legal obligations regarding fixed term contracts and statutory maternity provisions.
Please also note any secondment must first be agreed with your current line manager.
For further details / informal visits contact: Name: Nicola Tinker Job title: Senior Research Sister Email address: Telephone number:
I work cross site, and my additional contact number .
Please contact me to discuss any aspects of the Clinical Trials Assistant role.
The post holder will join the Clinical Trials Assistant (CTA) Team, with one of the Directorate Research Teams. The CTA Team work cross-site, to support the delivery of first class quality care to research participants within Sheffield Teaching Hospitals NHS Foundation Trust (STH). The CTA Team manage a portfolio of research studies that are conducted within STH Clinical Directorates and within the NIHR Sheffield Clinical Research Facility (CRF).
The post holder will assist in supporting a portfolio of clinical trials, from study set up to archiving, in accordance with clinical trial protocols, laboratory manuals and all relevant regulatory standards.
The role will involve completing and submitting documents to the Clinical Research and Innovation Office (CRIO) obtain approvals; collecting, recording and maintaining research data records; entering activity data and extracting information from databases, providing clinical and administrative support to Research Nurses including performing clinical tests and investigations, processing and shipping samples and assisting with screening and recruitment processes. Post holders may also support, and be responsible for, relevant studies in their own right.
You will be working for an organisation which values and respects all of its staff and the community it serves. The Trust is a leader in the NHS and research sectors and provides excellent benefits for its staff. This includes commitments to professional development but also many policies to support employees in balancing their personal and professional lives.
The CTA Team is part of the Clinical Research and Innovation Office (CRIO), and one of the Directorate Research Teams. It is involved in the delivery of clinical research across STH. We support the delivery of a wide range of studies, including studies from within the NIHR Sheffield Biomedical Research Centre (BRC) and NIHR Sheffield Clinical Research Facility (CRF).
This vacancy is advertised on a fixed term contract basis for a period of a maximum of twelve months due to maternity leave of the substantive post holder. The fixed term contract status of the post holder will be reviewed in accordance with the Trust's legal obligations regarding fixed term contracts and statutory maternity provisions.
Please also note any secondment must first be agreed with your current line manager.
For further details / informal visits contact: Name: Nicola Tinker Job title: Senior Research Sister Email address: Telephone number:
I work cross site, and my additional contact number .
Please contact me to discuss any aspects of the Clinical Trials Assistant role.
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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 Clinical Trials Assistant:
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To work as a Clinical Trials Assistant (CTA) in the UK, you'll need a combination of educational background, skills, and experience. Here are the key skills and qualifications typically required:
Educational Background:
- Degree: A degree in a scientific field such as life sciences, biomedical sciences, pharmacy, or a related subject is often preferred.
- Relevant Qualifications: Additional qualifications or certifications in clinical research or Good Clinical Practice (GCP) may be advantageous.
Key Skills:
1. Understanding of Clinical Trials: Familiarity with the clinical trial process, phases, and regulatory requirements.
2. Attention to Detail: Strong organizational skills and the ability to maintain accuracy in documentation and data entry.
3. Communication Skills: Excellent verbal and written communication skills for interacting with trial participants, medical staff, and other stakeholders.
4. Teamwork: Ability to work collaboratively in multidisciplinary teams.
5. Problem-Solving Skills: Capacity to identify issues and contribute to solutions in a clinical setting.
6. IT Proficiency: Proficiency with data management systems, databases, and Microsoft Office Suite. Ability to learn new software quickly is essential.
7. Time Management: Ability to prioritize tasks effectively and to meet deadlines, especially in a fast-paced environment.
8. Regulatory Knowledge: Understanding of ethical considerations and guidelines related to clinical research, including GCP and relevant legislation in the UK.
9. Analytical Skills: Competence in analyzing data and understanding trial metrics and results.
10. Adaptability: Flexibility and openness to learn and understand new procedures, protocols, and technologies.
Experience:
- Internships or Work Experience: Previous experience in a clinical research setting, even in temporary or voluntary roles, can be beneficial.
- Familiarity with Trial Protocols: Understanding the processes and documents associated with clinical trials, including informed consent forms, case report forms (CRFs), and study protocols.
Personal Attributes:
- Integrity and Ethics: A strong sense of professional ethics and the ability to handle sensitive information discreetly.
- Motivation and Enthusiasm: A genuine interest in clinical research and patient care.
Additional Considerations:
- Networking: Building a network with professionals in the field can provide opportunities and insights into job openings.
- Continuing Professional Development: Engaging in ongoing training and development in clinical research is valuable for career advancement.
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