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Clinical Trials AssistantinBournemouthinBournemouthPUBLISHED THU 12 DEC 2024

Band 3: £24,071 to £25,674 a year pa/pro rata  FIXEDTERM  GOOD SALARY 

CANCERNHSVENEPUNCTURE

University Hospitals Dorset NHS Foundation TrustFollow University Hospitals Dorset NHS Foundation Trust

Opportunity to contribute to groundbreaking research in oncology and improve patient outcomes.
Part of a supportive and enthusiastic team dedicated to high-quality, patient-centered clinical research.
Comprehensive training and development opportunities provided, making it suitable for entry-level candidates.
Ability to work across multiple specialties within University Hospitals Dorset, enhancing professional experience.
Friendly working environment that fosters collaboration with multidisciplinary teams.
Involvement in all aspects of the research process, providing diverse and engaging job responsibilities.
Flexibility in working locations, providing experience at both the Royal Bournemouth Hospital and Poole site.
The University Hospitals Dorset NHS Foundation Trust is seeking a motivated Clinical Trials Assistant to join their Research Department, specifically within the Oncology Research Team. This role will support the implementation of commercial and NIHR portfolio studies as part of The Early Cancer Diagnosis Programme and other oncology research initiatives. The successful candidate will engage in all aspects of the research process, including study start-up, recruitment, data collection, and close-out, while collaborating with multidisciplinary teams to enhance patient outcomes.

Candidates do not need prior research experience as comprehensive training will be offered; however, clinical skills such as venepuncture are a plus. Key qualities for applicants include a strong interest in clinical research, excellent communication and time management skills, attention to detail, and a self-motivated, flexible attitude. The position offers a friendly work environment with professional support and development opportunities, primarily based at the Royal Bournemouth Hospital with responsibilities at the Poole site as well.
Opportunity to contribute to groundbreaking research in oncology and improve patient outcomes.
Part of a supportive and enthusiastic team dedicated to high-quality, patient-centered clinical research.
Comprehensive training and development opportunities provided, making it suitable for entry-level candidates.
Ability to work across multiple specialties within University Hospitals Dorset, enhancing professional experience.
Friendly working environment that fosters collaboration with multidisciplinary teams.
Involvement in all aspects of the research process, providing diverse and engaging job responsibilities.
Flexibility in working locations, providing experience at both the Royal Bournemouth Hospital and Poole site.

Here are 5 questions you could be asked if you apply for this job: Start practice interview...
1. What inspired you to apply for the Clinical Trials Assistant role, and what interests you most about clinical research?
2. Can you describe a situation in which you demonstrated initiative in a previous role or project?
3. This role requires excellent communication skills. Can you provide an example of how you effectively communicated complex information to a non-expert audience?
4. How would you approach explaining a clinical trial to a patient who is hesitant or anxious about participating?
5. In clinical research, attention to detail is crucial. Can you describe a time when your focus on detail helped prevent a potential issue or mistake in your work?
See all questions
1. What inspired you to apply for the Clinical Trials Assistant role, and what interests you most about clinical research?
2. Can you describe a situation in which you demonstrated initiative in a previous role or project?
3. This role requires excellent communication skills. Can you provide an example of how you effectively communicated complex information to a non-expert audience?
4. How would you approach explaining a clinical trial to a patient who is hesitant or anxious about participating?
5. In clinical research, attention to detail is crucial. Can you describe a time when your focus on detail helped prevent a potential issue or mistake in your work?
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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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