Detailed job description and main responsibilities

PRIMARY DUTIES & AREAS OF RESPONSIBILITY
Leadership
1. Have an understanding of the clinical research team work-plan and contribute to its achievement. 
2. Manage research performance and study timelines of relevant studies. 
3. Collaborate with other Trusts and organisations within the region to improve research delivery. 
4. Keep up to date with research management issues through liaison with other Research Specialists /Team leaders and link with national networks. 
5. Provide relevant supervision and mentorship to members of staff and students. 
6. Take responsibility for own health, safety and security and promote the health, safety and security of the wider team. 
7. Contribute to the development and implementation of clinical and research policies, procedures and SOPs. 
8. Facilitate and maintain effective communication within the research team and between the multidisciplinary clinical team. 
9. Assist in the delivery of education and training regarding research for the wider Multidisciplinary Team and act as an ambassador for research. 
10.Promote a blame free culture in reporting incidents and where appropriate support local investigation of incidents.
11.Support appropriate studies within PHNT/UHP and its partner organisations as appropriate.

Research 
1. Be responsible for the delivery of a clinical trial portfolio relevant to the specialty. 
2. Ensure that the delivery of studies meet requirements with regards to the Department of Health’s Research Governance Framework for Health & Social Care and the EU Clinical Trials Directive by implementing quality systems. 
3. Participate in Good Clinical Practice (GCP) training. 
4. Contribute to the Expression of Interest / Study Selection process for the relevant specialty. 
5. Contribute to study set up, recruitment planning and study delivery. 
6. Lead forward and contribute to Patient and Public involvement activities. 
7. Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies. Work with the clinical trials team and investigators to develop strategies to overcome barriers to recruitment and to solve other problems relating to specific studies. 
8. Coordinate and run study visits including off site visits whilst adhering to the lone worker policy. 
9. Work with other departments within the Trust to ensure that trial specific investigations and procedures are undertaken as required by the trial protocol, in order to establish eligibility and safety of patients within clinical trials. 
10.Contribute to the accurate costing for clinical trials 
11.Ensure clear, accurate and concise records are kept for research projects in accordance with all regulatory requirements including the Data Protection Act. 
12.Ensure that data is transcribed accurately where required and assist with the maintenance of the Trial Master File. 
13.Respond to data queries generated by the study coordinating team within a timely manner. 
14.Ensure the recording & reporting of adverse and serious adverse events that occur whilst the participant is in the clinical trial to the trial co-coordinator/Principal Investigator (PI) and R&D office in line with the study protocol, local policies and regulatory requirements. 
15.Assess and evaluate the progress of on-going clinical trials for which the post holder has responsibility, maintaining accurate records of the status of studies and providing regular updates to the department on the status of the studies. This will involve ensuring that any Data Management Systems are updated with key trial data and validated efficiently.
16.Escalate on-going study performance issues to the Senior Research Nurse or Team Lead. 
17.Co-operate with external and internal audit, data monitoring and quality assurance by working with R&D, sponsors, study monitors and external bodies. 
18.Assist in study close down and the preparation of results of research for presentation as posters, abstracts, papers or scientific presentations.

Clinical & Professional 
1. Be responsible for the care of research participants within the relevant sphere of practice and use opportunities to provide health promotion and patient education. 
2. Use relevant clinical knowledge to screen and identify patients suitable for clinical research using inclusion and exclusion criteria and utilising NHS records, screening clinics, visiting wards and outpatients and using Trust IT systems and databases. 
3. Act as a resource and role model for all aspects of Research Clinical Practice in order to optimise patient care and clinical practice this may include carrying out physical assessments, conducting sample retrieval and processing, providing or coordinating interventions and treatments, clinical monitoring. 
4. Undertake all mandatory training and take part in personal development reviews. 
5. Ensure the environment is suitable for patient care and research processes, recognising the importance of privacy, dignity and diversity. 
6. Demonstrate professional development and an in-depth knowledge of current clinical and research practice. 
7. Provide on-going advice and information to patients and their carers/families with regard to their participation in clinical research in order to facilitate effective informed consent. 
8. Where appropriate receive and document written informed consent from research subjects. Training and support for informed consent will be given. 
9. Be responsible for the safe and accurate collection of research data through clinical procedures such as venepuncture, history taking, standard observations (height, weight, BP, RR, HR, SpO2 temperature) and other assessments such as ECG, physical examinations, disease specific outcome measures, questionnaires, rated scales, qualitative interviewing as required by the protocol. 
10.Centrifuge, process track and ship samples in line with protocol requirements. 
11.Ensure the safe administration of any treatments and drugs given within the context of a clinical trial. 
12.Monitor treatment toxicity/side effects and initiate changes to treatment as required by the protocol. Escalate any concerns to the Principle Investigator or relevant physician. 
13.Ensure accurate patient trial documentation, including the use of electronic data capture systems and ensure relevant information is recorded in patients’ medical notes and case report form in a timely manner. 
14.Refer to other specialists as required in order to provide optimal care of the participant. 
15.Contribute to the monitoring of clinical standards within the research team. 
16.Treat all persons encountered during the course of duties with respect and courtesy and maintain a standard of conduct which best represents the clinical trials team and the Trust. 
17.Work within the relevant professional code of conduct (if applicable) demonstrating accountability for own actions and awareness of own limitations. 
18.Provide cover for other research nurses/ practitioners as required. 
19.Proactively seek feedback from participants and their families during their research involvement.
20.Contribute to Patient and Public Involvement and Engagement activities across the department