199529 Clinical Trials Assistant (SNIS) inEdinburgh inEdinburgh PUBLISHED 18 OCT 2024
NHS Scotland rvrQq6u
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For further information on what is included in the role and what skills/experience are being looked for, click on the links at the bottom of the screen to the job description and person specification.
NHS Scotland is committed to encouraging equality and diversity among our workforce and eliminating unlawful discrimination. The aim is for our workforce to be truly representative and for each employee to feel respected and able to give their best. To this end, NHS Scotland welcomes applications from all sections of society.We will fully support disabled candidates, and candidates with long-term conditions or who are neurodivergent by making reasonable adjustments to our recruitment policy and practices.
Job Purpose
The post holder will assist with the delivery of direct and indirect clinical and research care, sample processing support for research studies/trials. The post holder will assist with the general administrative requirements associated with study set up, running and closing of a clinical trial including data collection, data entry maintenance of essential documents. All work undertaken in the Department, is in accordance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP) to ensure provision of high quality care
The post holder will carry out assigned clinical duties under direct and indirect supervision of senior nursing staff other relevant professional practitioners to provide, through Divisional policies, a safe environment for the treatment of research subjects, and the protection of staff.
For further information on what is included in the role and what skills/experience are being looked for, click on the links at the bottom of the screen to the job description and person specification. If after reading this information you have any questions please contact Anna Miell on or
**Please note we anticipate a high level of interest in this position and may close the vacancy early once a sufficient amount of applications are received. Therefore, please make sure you complete and submit your application at an early stage**
NHS Scotland is committed to encouraging equality and diversity among our workforce and eliminating unlawful discrimination. The aim is for our workforce to be truly representative and for each employee to feel respected and able to give their best. To this end, NHS Scotland welcomes applications from all sections of society.
We will fully support disabled candidates, and candidates with long-term conditions or who are neurodivergent by making reasonable adjustments to our recruitment policy and practices.
Job Purpose
The post holder will assist with the delivery of direct and indirect clinical and research care, sample processing support for research studies/trials. The post holder will assist with the general administrative requirements associated with study set up, running and closing of a clinical trial including data collection, data entry maintenance of essential documents. All work undertaken in the Department, is in accordance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP) to ensure provision of high quality care
The post holder will carry out assigned clinical duties under direct and indirect supervision of senior nursing staff other relevant professional practitioners to provide, through Divisional policies, a safe environment for the treatment of research subjects, and the protection of staff.
For further information on what is included in the role and what skills/experience are being looked for, click on the links at the bottom of the screen to the job description and person specification. If after reading this information you have any questions please contact Anna Miell on or
**Please note we anticipate a high level of interest in this position and may close the vacancy early once a sufficient amount of applications are received. Therefore, please make sure you complete and submit your application at an early stage**
We will fully support disabled candidates, and candidates with long-term conditions or who are neurodivergent by making reasonable adjustments to our recruitment policy and practices.
Job Purpose
The post holder will assist with the delivery of direct and indirect clinical and research care, sample processing support for research studies/trials. The post holder will assist with the general administrative requirements associated with study set up, running and closing of a clinical trial including data collection, data entry maintenance of essential documents. All work undertaken in the Department, is in accordance with the International Conference on Harmonisation Good Clinical Practice Guidelines (ICH-GCP) to ensure provision of high quality care
The post holder will carry out assigned clinical duties under direct and indirect supervision of senior nursing staff other relevant professional practitioners to provide, through Divisional policies, a safe environment for the treatment of research subjects, and the protection of staff.
For further information on what is included in the role and what skills/experience are being looked for, click on the links at the bottom of the screen to the job description and person specification. If after reading this information you have any questions please contact Anna Miell on or
**Please note we anticipate a high level of interest in this position and may close the vacancy early once a sufficient amount of applications are received. Therefore, please make sure you complete and submit your application at an early stage**
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Useful skills for a 199529 Clinical Trials Assistant (SNIS):
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To work as a Clinical Trials Assistant (CTA) in the UK, particularly under the National Occupational Classification code 199529 (Clinical Trials Assistant - Standard Occupational Classification), you'll need a combination of educational qualifications, technical skills, and soft skills. Here are some key skills and qualifications that are typically required for this role:
Educational Qualifications:
1. Degree in a Relevant Field: Usually, a degree in life sciences, healthcare, or a related field is preferred. Some roles may accept candidates with A-levels and relevant experience.
2. Knowledge of Clinical Research: Understanding of clinical trial protocols, phases of clinical trials, and regulatory requirements is crucial.
Technical Skills:
1. Familiarity with Clinical Trial Regulations: Understanding of Good Clinical Practice (GCP), the Medicines and Healthcare products Regulatory Agency (MHRA) guidelines, and other regulatory requirements.
2. Data Management Skills: Ability to manage study-related documentation, data entry, and maintaining accurate records.
3. Knowledge of Medical Terminology: Familiarity with medical vocabulary is often beneficial.
IT Skills:
1. Proficiency in MS Office: Strong skills in Microsoft Word, Excel, and PowerPoint for report generation and data analysis.
2. Clinical Trial Management Systems (CTMS): Familiarity with software used for managing clinical trials can be an advantage.
Soft Skills:
1. Attention to Detail: Precision and accuracy are vital in clinical trials to avoid errors in documentation and data.
2. Organizational Skills: Ability to manage multiple tasks, deadlines, and priorities efficiently.
3. Communication Skills: Strong written and verbal communication skills for interacting with team members, researchers, and participants.
4. Problem-Solving Skills: Ability to identify issues and find solutions proactively.
Experience:
1. Previous Experience: While not always required, experience in a clinical research environment, administrative roles, or laboratory settings can be advantageous.
2. Internships or Volunteer Work: Participating in internships or volunteering in research or healthcare settings can provide practical experience.
Certifications:
1. Good Clinical Practice (GCP) Certification: Having GCP training is often expected or required, as it demonstrates knowledge of ethical and scientific quality standards for designing, conducting, recording, and reporting trials.
Additional Attributes:
1. Teamwork: Ability to work effectively in a team-oriented environment.
2. Adaptability: Being flexible and able to adjust to changing project conditions.
inEdinburgh
55.953250885009766 -3.1882669925689697 Edinburgh, Scotland, United Kingdom 
Locations are approximate.
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