Job summary
Please see detailed job description with particular reference to the key responsibilities such as: clinical, research, communication, education.
Main duties of the job
Please check the job description document for more information on the requirements for this job with particular attention to the clinical responsibilities.
About us
Surrey and Borders Partnership NHS Foundation Trust is the leading provider of health and social care services for people of all ages with mental ill-health and learning disabilities in Surrey and North East Hampshire. We also provide social care services for people with a learning disability in Croydon and ASD and ADHD assessment services in Hampshire.
We actively seek to engage people who use our services and our communities in improving the mental wellbeing of the local population. We work closely with other NHS and voluntary sector organisations who provide services and support people who use services and carers.
Surrey is a beautiful county lying just 30 minutes away from Central London and from the South Coast.
Our historic market towns and bustling districts are enveloped in wonderful countryside, and our excellent road and rail networks bring the rest of the country within easy reach.
For international travel, both Gatwick and Heathrow airports are nearby.
Please note that we reserve the right to close posts as soon as sufficient applications are received.
We look forward to receiving your application!
Job description
Job responsibilities
Please see detailed job description for full responsibilities.
Clinical Work autonomously and assist in the management of a caseload of clinical trial participants whilst working as part of a multi-disciplinary team. Maintain effective communication with people who use our services, carers and professionals to ensure high quality service delivery Identify suitable people who use our services for entry into clinical trials Maintain accurate documentation of participants events in progress notes Ensure people who use our services are fully informed prior to entry into clinical trial programmes Provide ongoing information, education and support to participants (and their significant others) regarding clinical trials and specific trial treatments Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain results in order to establish eligibility and safety to enter the trial Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocols Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authorities Provide continuity of care to participants and their carers throughout the trial programme. Provide specific advice and psychological support as appropriate. Refer to other specialists as required to ensure optimum participants care. Act as a primary contact point for the trial participant Maintain accurate participants trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in participants case notes
Person Specification
essential
Essential
1. minimum 2 years post qualification experience
Desirable
2. More than 2 years previous research experience
essential
Essential
3. NHS experience
Desirable
4. previous work experience
desirable
Desirable
5. previous research experience
driving licence
Essential
6. uk valid driving licence and car owner
Desirable
7. uk valid driving licence