Clinical Research Practitioner

7 days ago

Nottingham, United Kingdom Nottingham University Hospitals NHS Trust Full time

**Job overview**:
Are you interested in Audiology & ENT clinical trials and working within a dynamic growing team. If so, an exciting opportunity is now available within the Research and Innovation Department at Nottingham University Hospitals (NUH) based between the Ropewalk and QMC sites.

The post holder will be supporting the coordination and running of complex clinical trials for both commercial and non-commercial and other types of clinical research in the Trust. You will need knowledge of / experience of delivering clinical research studies in a clinical setting.

The post-holder will be required to work flexibly over a five day week. Occasional out of hour’s working (including weekends) may be required.

**Main duties of the job**:
**In addition to the below summary you need to familiarize yourself with full Job Description and Person Specification documents attached to this advert.**

**Clinical**

Assist research nurses/ACP’s/Clinicians in delivery of patient care to research participants.

Support and co-ordinate obtaining and processing of blood and tissue samples in the clinical setting as well as optimising recruitment via clinics and MDT’s.

Work alongside research nurses ensuring samples are collected and recorded per protocol.

Review and record treatments, adverse events and response to treatment to relevant study documentation including source data and case report forms including electronic data entry.

Plan, prepare and participate in monitoring visits and respond to trial data queries.

**Working for our organisation**:
NUH hosts hundreds of clinical research studies every year, including complex clinical trials. More than 300 doctors, nurses and health professionals are involved in clinical research, ensuring that the benefits of new treatments, drugs and therapies translate from the research laboratory directly into clinical practice.

Through our research we will make a real and lasting difference to the quality of clinical care provided by NUH, building on existing strengths and exploiting new opportunities. We do this through partnerships which support research locally, nationally and internationally. NUH also works in close partnership with The Clinical Research Network East Midlands (CRN East Midlands) who are part of the NIHR Clinical Research Network and aims to improve the speed, quality, and integration of clinical research, through the successful delivery of clinical studies in the NHS.

**Detailed job description and main responsibilities**:**Communication**
To function as a member of the Research and Innovation Clinical Trials Team to provide dedicated clinical trials support to research teams across NUH. Working within a multi-disciplinary team, to co-ordinate a caseload of patients participating in local, national and international clinical trials in various treatment types.

Disseminate information to consultants regarding new trials on the National Institute of Health Research trial portfolio as well as non-adopted clinical trials, to enable optimal patient recruitment.

Ensure ethics and R&D approval and indemnities are in place before recruitment of first patients to a newly set up trial. Facilitate the set-up of trials on site i.e. SSI submission via IRAS account, liaise with trial centre and other relevant staff to organise trial set-up visits.

Liaise with clinical teams to organise and ensure that trial specific investigations are undertaken as and when required, obtain the results, ensure eligibility and randomise the patient.

Liaise with medical staff to record organise and ensure the timely administration of treatment and any necessary follow up investigations and visits.

Liaise with histopathology ensuring tissue samples are stored via Tissue Bank guidelines, organising storage and catalogue of samples kept.

To ensure effective communication with support departments to request and obtain specific trial related information. E.g. Radiology copy scans, histological status and tissue samples.

Organise the collection, storage and shipment of protocol specific samples. Explain, dispense and collect patient quality of life questionnaires and diaries. Liaise with designated Pharmacist to co-ordinate the availability and dispensing of trial drugs if required.

Provide information to allow for invoices to be raised for payments where appropriate.

Contribute to and supply verbal and written information on the teams portfolio of trials and the number of patients recruited to the R&I team, hospital/university staff, local/Network meetings, regulatory bodies etc., as required.

**Person specification**:
**essential**:
**Essential criteria**:

- Educated to Diploma level or relevant experience

**Desirable criteria**:

- GCP training

**Experience**:
**Essential criteria**:

- Working in a clinical NHS setting

**Desirable criteria**:

- Clinical Trials Experience

**Skills**:
**Essential criteria**:

- Able to assess and interpret clinical/non-clinical informati

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