Clinical Trials Assistant inBolton inBolton PUBLISHED THU 7 NOV 2024

Band 3: £24,071 to £25,674 a year Per annum FIXEDTERM GOOD SALARY

CASELOAD NHS

Bolton NHS Foundation Trust rEn7pDMh

The Bolton NHS Foundation Trust is seeking a motivated Clinical Trials Assistant to join their Research and Development team at the Royal Bolton Hospital on a temporary 12-month contract. The role involves providing vital administrative support for clinical trials, working closely with research nurses and other practitioners on a defined portfolio of studies. Key responsibilities include maintaining trial site files, collecting and inputting research data, facilitating communication with study sponsors and researchers, and assisting with laboratory tasks.

Candidates must possess strong organisational skills, attention to detail, and the ability to work independently while ensuring a high-quality research service. The position demands accuracy and the capacity to meet deadlines, making it essential for applicants to be enthusiastic about contributing to the growth of research within the Trust.

Band 3 - Clinical Trials Assistant

Temporary Contract - 12 Months

Base: Research and Development, Royal Bolton Hospital

In order to support the growth and development of Research across the Trust, we are looking for an enthusiastic and highly motivated individual to join our Research team in the role of Clinical Trials Assistant.

The Clinical Trials Assistant works closely with the research nurses and practitioners who are responsible for the management of a defined portfolio of research studies and caseload of patients participating in clinical trials.

The post-holder will support the clinical team by providing comprehensive administrative support relating to trials. The role will involve maintenance of trial site files, collection and input of research data, communication with study sponsors, researchers and the research network to assist with the set-up of new trials, and some basic laboratory support. They will be expected to work at times without supervision and at all times to facilitate a high quality research service. We are looking for someone with excellent organisation skills and attention to detail, who can work to deadlines with accuracy.

About us
Full details of the post responsibilities can be found in the job description and person specification provided.

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Useful skills for a Clinical Trials Assistant: Click to view

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.

Clinical Trials Assistant inBolton inBolton PUBLISHED THU 7 NOV 2024

Bolton NHS Foundation Trust rEn7pDMh

About us Full details of the post responsibilities can be found in the job description and person specification provided.

About us
Full details of the post responsibilities can be found in the job description and person specification provided.