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Clinical Trials AssistantinBoltoninBoltonPUBLISHED THU 7 NOV 2024

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

CASELOADNHS

Bolton NHS Foundation TrustFollow Bolton NHS Foundation Trust

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.

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Useful skills for a Clinical Trials Assistant:
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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