Clinical Research Officer

2 months ago

Nottingham, United Kingdom Nottingham University Hospitals NHS Trust Full time

5

**Main area**
- Research & Innovation

**Grade**
- 5

**Contract**
- Permanent: Secondment 1 year will be considered

**Hours**
- Full time - 37.5 hours per week (The post holder is expected to work flexibly over 7 days a week to cover the service)

**Job ref**
- 164-6103121

**Site**
- Queens Medical Centre

**Town**
- Nottingham

**Salary**
- £28,407 - £34,581 Per Annum Pro Rata

**Salary period**
- Yearly

**Closing**
- 01/04/2024 23:59

Job overview

Main duties of the job

In addition to the brief list below you must familiarise yourself with the full job description and person specification attached to this advert prior to applying.
- To coordinate the care of your own caseload of clinical trial participants
- To attend Multi-disciplinary meetings, and appropriate clinics, to screen and recruit new participants.
- Ensure safe administration of treatments and medications, given within the context of a clinical trial and within the scope of relevant professional practice.
- To ensure that trial specific investigations are undertaken as required by the trial protocol, in order to establish eligibility and safety to enter the trial.
- To provide ongoing information, education and support to children, carers and families regarding clinical studies.
- To ensure blood and other samples are collected for pharmacokinetic studies as required by the trial protocol.
- To monitor treatment toxicity/side effects.
- To maintain accurate documentation of research related activities.
- To accurately record data collected in the Case Report Forms.
- To record and report adverse events to the relevant personnel and take any necessary action.
- To report and record serious adverse events to relevant local personnel / Regulatory Authorities.
- To follow appropriate Trust Policies and Procedures and to ensure that you are working according to Good Clinical Practice and Research Governance standards for clinical studies

Working for our organisation
- **Patients**:

- We will ensure our patients receive consistently high quality, safe care with outstanding outcomes and experience
- **People**:

- We will build on our position as an employer of choice; with an engaged, developed and empowered team that puts patient care at the heart of everything it does
- **Places**:

- We will invest in our estate, equipment and digital infrastructure to support the delivery of high quality patient care
- **Performance**:

- We will consistently achieve our performance standards and make the best use of resources to contribute to an affordable healthcare system
- **Partners**:

- We will support the improvement of the health of the communities we serve through strong system leadership and innovative partnerships to deliver integrated models of care
- **Potential**:

- We will deliver world-class research and education and transform health through innovation

Detailed job description and main responsibilities

**Clinical**
- To coordinate the care of your own caseload of clinical trial participants
- To attend Multi-disciplinary Meetings, and appropriate clinics, to screen and recruit new participants, and to act as a resource to the members of the MDT.
- To ensure the safe administration of treatments and medications, given within the context of a clinical trial and within the scope of relevant professional practice.
- To ensure that trial specific investigations are undertaken as required by the trial protocol, in order to establish eligibility and safety to enter the trial.
- To provide ongoing information, education and support to children, carers and families regarding clinical studies.
- To ensure blood and other samples are collected for pharmacokinetic studies as required by the trial protocol.
- To monitor treatment toxicity/side effects and initiates changes to treatment as required by the protocol within the scope of relevant professional practice.
- To maintain accurate documentation of research related activities in Study, Nursing and Medical notes.
- To accurately record data collected in the Case Report Forms (CRF).
- To record and report adverse events to the relevant personnel and take any necessary action.
- To report and record serious adverse events to the Trial Co-coordinator/Principal Investigator (PI) and relevant local personnel / Regulatory Authorities.
- To follow appropriate Trust Policies and Procedures and to ensure that you are working according to Good Clinical Practice and Research Governance standards for clinical studies

**Clinical Research**
- Responsible for assessment of research care needs, the planning, implementation and evaluation of care delivered, so that patients’ individual requirements for research care are met.
- Carry out policies and procedures in accordance with agreed Trust policies and standards.
- Be aware of and adhere to Trust policy for Administration of Medicines where relevant to professional boundaries.
- Demonstrate initiative and competence in all clinical procedures under

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