Clinical Trials Assistant inBasingstoke inBasingstoke PUBLISHED WED 20 NOV 2024

Band 4: £26,530 to £29,114 a year pro rata per annum PERMANENT GOOD SALARY

MULTI-DISCIPLINARY NHS

Hampshire Hospitals NHS Foundation Trust r2wpy08B

Part-time schedule with flexibility, allowing for a better work-life balance.

Opportunity to work within a multidisciplinary team, gaining diverse experiences and insights from various healthcare professionals.

Provision of comprehensive training, making the role suitable for individuals without prior experience in research.

Engagement in meaningful work by supporting clinical trials that can lead to advancements in medical research and patient care.

Work in a dynamic and fast-paced environment, which can enhance personal and professional growth.

Possibility to develop new skills in research delivery and data management, boosting career prospects.

Contribute to the successful running of clinical trials in a reputable NHS Foundation Trust, enhancing the quality of healthcare services in the community.

The role of Clinical Trials Assistant at Hampshire Hospitals NHS Foundation Trust in Basingstoke is a part-time position (30 hours per week, over 4 days) aimed at established healthcare or administrative staff seeking to expand their experience in research delivery. The successful candidate will support a multidisciplinary team of research nurses and practitioners in managing both commercial and non-commercial clinical trials. Key responsibilities include data management, administrative tasks, clinical support, collecting trial data, and assisting in the setup and management of trials while adhering to Good Clinical Practice and standard operating procedures.

Candidates do not need prior research experience, as full training will be provided. Ideal applicants will possess a proactive attitude, the ability to work well under pressure, and strong time management skills. The role emphasises teamwork and a flexible approach in a fast-paced environment to ensure the successful execution of clinical trials.

Part time - 30 hours per week (4 working days to be decided, some cross-site working)

Are you an established health care staff member looking for a new experience and development opportunity?

Or are you working in administration but wish to utilise your existing skills and develop new skills in research delivery?

The research department has a vacancy for a Band 4 Clinical Trials Assistant to support research nurses, AHPs and practitioners with a portfolio of commercial and non-commercial clinical trials and research studies. You will be part of a multidisciplinary team including experienced medical, nursing, administrative and support staff supporting an exciting range of studies across different specialties.

Experience in research would be advantageous but not essential - full training will be provided.

The main purpose of the role is to provide data management, administrative and some clinical support for clinical trial activities according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies in the Hampshire Hospitals NHS Foundation Trust R & D department. The post holder will provide support to the clinical team in trial activities including collecting trial data, completing data collection forms, assisting in the set-up of new trials and ongoing management of existing trials and assisting in workload management in both an administrative and clinical capacity. The department is involved in a wide portfolio of clinical trials and the post-holder will work closely with the multi-disciplinary team to deliver the trials to a high standard.

About us
We are looking for an interested and enthusiastic person who can work well under pressure and as part of a team but also able to manage his/her time appropriately. This person needs to have a good common sense approach to life and be able to work flexibly and calmly in a fast paced environment. The post holder will provide administrative and some clinical support to the Research team enabling the successful running of clinical trials in a healthcare setting.

Further information about the Trust and this role can be found on the Job Description and Person Specification document attached.

All shortlisted candidates are expected to attend for an informal visit as part of the interview process, which should be arranged in advance.

More information related to this job opportunity, from jobsincare:

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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.

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