Band 6 Research Nurse - The Barberry Centre

at  Birmingham and Solihull Mental Health NHS Foundation Trust

Working predominantly at the Barberry Centre, at Birmingham and Solihull Mental Health NHS Foundation Trust (BSMHFT), the post-holder will support the regional Mental Health Mission to Midlands Translational Research Centre of Excellence to increase recruitment to mood disorders studies, predominantly for people experiencing depression.

For any assigned project, they will be responsible for assessing and managing the care pathways for patients and carers participating in clinical studies. This will involve the recruitment, education and monitoring of trial patients and the collection and documentation of accurate data, including the collection and preparation of samples. You will work collaboratively with the research delivery team and the wider multi-disciplinary team in the management of your own caseload of clinical trial patients. The role involves using an in-depth knowledge of trial protocols and their application in practice, alongside a working knowledge and compliance with the local, national and international research regulations and nursing framework. This post would suit someone with a clinical background in nursing and previous hands on clinical trial/research experience is a must. Experience of working in a mental health setting or with patients experience depression would be desirable.

• Coordinate the care of your own case load of clinical trial patients
• Ensure the safe administration of treatments given within the context of a clinical trial
• Conduct assessments with study participants based upon competency and study specific training
• Take clinical samples for studies; coordinate tissue sample collection and dispatch to relevant departments or research centres
• To ensure that trial specific investigations are undertaken as required by the research protocol
• To provide on-going information, education and support to patients (and their carers) regarding clinical trials
• To maintain accurate documentation of patient events in nursing, medical and trial notes
• To act appropriately to report and record serious adverse events, this includes communication with the Principal Investigator and relevant local personnel and regulatory authorities
• To provide on-going follow up care whilst patient is in the clinical trial
• Act at all times in a way that maintains patients’ and carers’ dignity
• Refer to other specialists as required in order to provide optimal patient care
• Unless otherwise agreed, act as a primary contact point for the clinical trial patient
• Identify patients suitable for entry into clinical trials by attending ward rounds, clinics (screening notes/consultant referral) and Multi-disciplinary Team (MDT) meetings

Welcome to Birmingham and Solihull Mental Health NHS Foundation Trust. Our 4000 clinical and support staff help us to improve mental health wellbeing and meet the needs of the 70,000 people we serve each year. We provide a range of mental healthcare services across Birmingham and Solihull, as well as specialised services nationally. We also offer medical, nursing and psychology training and are proud of our international reputation for both research and innovation.
Our population is culturally diverse, characterised in places by high levels of deprivation which create an increasing demand for our services and a necessity for us to make sure everyone can access the help they need. We are a team of compassionate, inclusive and committed people working together to provide excellent care to support our community. If you are looking for a place to belong, where you can make a real difference to people’s lives, join our team where our warm welcome is waiting for you.
For further information about the main responsibilities, please view the attached job description and person specification

• Coordinate the care of your own case load of clinical trial patients
• Ensure the safe administration of treatments given within the context of a clinical trial
• Conduct assessments with study participants based upon competency and study specific training
• Take clinical samples for studies; coordinate tissue sample collection and dispatch to relevant departments or research centres
• To ensure that trial specific investigations are undertaken as required by the research protocol
• To provide on-going information, education and support to patients (and their carers) regarding clinical trials
• To maintain accurate documentation of patient events in nursing, medical and trial notes
• To act appropriately to report and record serious adverse events, this includes communication with the Principal Investigator and relevant local personnel and regulatory authorities
• To provide on-going follow up care whilst patient is in the clinical trial
• Act at all times in a way that maintains patients’ and carers’ dignity
• Refer to other specialists as required in order to provide optimal patient care
• Unless otherwise agreed, act as a primary contact point for the clinical trial patient
• Identify patients suitable for entry into clinical trials by attending ward rounds, clinics (screening notes/consultant referral) and Multi-disciplinary Team (MDT) meeting