Job summaryClinical Research PractitionerDivision: Corporate
Care Group: Medical Directorate
Band: 5
Salary: £29,970 - £36,483 per annum
Working as part of the R&I Department, the post holder will assist in delivery of the Trust's research portfolio. The individual will assist in management of research projects and this can include: set up processes (leading to confirmation of capacity and capability), delivery of agreed recruitment target, addressing any queries. Will liaise with external and internal researchers and institutions to advise about Trust research processes and promote Trust research activities. All activities must be undertaken in accordance with the NHS, Trust and other relevant policies and procedures, ensuring the well-being of participants within research at all times.
The Department is committed to meeting national, local, contractual and other deadlines and post holder is expected to contribute to achieving these.
The post is funded by the SE Regional Research Delivery Network (SE RRDN) and only supports research activities. This does not include the delivery of any aspect of standard clinical care.
Main duties of the jobThe Research and Innovation Department at Medway Hospital is a growing area with an excellent reputation. Since 2013, the Trust R&I contributed the highest number of participants in clinical research among the other organisations in Kent, Surrey and Sussex Clinical Research Network.
We aim to offer as many patients as possible the opportunity to take part in cutting edge research, allowing them to receive and contribute to the treatments of the tomorrow.
Our values are
Bold,
Every Person Counts,
Sharing and Open and
Together. It is important that you understand and to refer to our values when completing your application and always reflect our values throughout your employment with the Trust.
We are committed to endorsing diversity, multiculturalism, and inclusion; our policies / procedures ensure that all applicants are treated fairly at every stage of the recruitment process.
To contribute to our exciting future and become part of our team, apply today.
About usDo you have the ambition and vision to deliver our mission of theBest of Care by the Best of People providing excellent care, every time?Here at Medway, we pride ourselves on working together as one to ensure that our shared
vision is achieved for our patients.
As a key partner in the healthcare of our local population, we are keen to deliver this as an outcome of our Trust-wide strategy -
Patient First. Using an Operational Excellence approach to align our priorities and operational management structures, we are just over a year and half into our
Patient First deployment. We are looking for creative, skilled people to join our Transformation Team and further support us on this journey.
Our culture and values define us here at Medway NHS Foundation Trust and are the heartbeat of who we are as an organisation.
Our
BEST values underpin
Patient First and are at the core of the care we give to our patients, the support we offer to our staff and our overall leadership approach:
B - BoldE - Every person countsS - Sharing and openT - TogetherOur Trust is a great choice for people who want to develop their career in an ambitious and dynamic environment; our employees are able to choose the coverage and supplemental benefits that best fit their needs and those of their families. This includes the promotion of flexible working opportunities across the Trust.
Job descriptionJob responsibilitiesWill assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets
Assist in the delivery of recruitment targets in line with the contractual agreements, agreed time lines
Open and manage allocated projects, set timescales and resolve problems. This includes management of the set up process
Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies
Maintain accurate records of portfolio activities
Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs)
Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit
Job description
Job responsibilitiesWill assist in the management of research projects providing the necessary support so that studies can be set up and conducted safely, efficiently according to the required standards & targets
Assist in the delivery of recruitment targets in line with the contractual agreements, agreed time lines
Open and manage allocated projects, set timescales and resolve problems. This includes management of the set up process
Take responsibility for all areas of practice relating to the conduct of clinical trials and research studies
Maintain accurate records of portfolio activities
Under supervision, report, address, help to resolve any breaches and protocol deviations. Report Adverse Events (AEs) using appropriate procedures, including the expedited reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs)
Prepare/assist with preparation of patient documentation for research-related treatment clinics, complete accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit
Person SpecificationQualificationsEssential- Good level of education
- Preferably 1st Degree/Diploma in Health Science, Nursing or other relevant subject
- Alternatively experience in research pharma or other health/research related institution will be considered
KnowledgeEssential- Understanding of health research in the UK
- Knowledge of Research Governance Framework, Medicines for Human Use Regulations, Good Clinical Practice and the Health Research Authority (HRA)
ExperienceEssential- Experience in assisting/participating in a research trial or similar
- Experience of working in NHS setting or other research environment
SkillsEssential- Ability to prioritise workload and manage own time effectively
- Excellent written and oral communication skills
- Proven organisation skills
- Ability to develop new skills
- Excellent interpersonal skills
Person Specification
QualificationsEssential- Good level of education
- Preferably 1st Degree/Diploma in Health Science, Nursing or other relevant subject
- Alternatively experience in research pharma or other health/research related institution will be considered
KnowledgeEssential- Understanding of health research in the UK
- Knowledge of Research Governance Framework, Medicines for Human Use Regulations, Good Clinical Practice and the Health Research Authority (HRA)
ExperienceEssential- Experience in assisting/participating in a research trial or similar
- Experience of working in NHS setting or other research environment
SkillsEssential- Ability to prioritise workload and manage own time effectively
- Excellent written and oral communication skills
- Proven organisation skills
- Ability to develop new skills
- Excellent interpersonal skills
Disclosure and Barring Service CheckThis post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of SponsorshipApplications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the .
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. .
UK RegistrationApplicants must have current UK professional registration. For further information please see
Additional information
Disclosure and Barring Service CheckThis post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of SponsorshipApplications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the .
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. .
UK RegistrationApplicants must have current UK professional registration. For further information please see
Employer detailsEmployer nameMedway NHS Foundation Trust
AddressMedway NHS Foundation Trust
Windmill Road, Gillingham
Kent
ME7 5PN
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