Job summaryThe Research & Innovation Team is a busy department, offering support to many academic and commercial reserach trials either in progress or in set-up. We are also aiming to begin to undertake more 'home-grown' research. In order to ensure we are compliant with the requirements of the projects, national research policy guidelines, and Good Clinical Practice (GCP) guidelines., we are looking for an enthusiastic, organised and methodical individual to provide direct administrative support to the clinical delivery team.Main duties of the jobWorking within research is a challenging yet rewarding role which involves supporting projects that will potentially impact on patient treatments of the future. There will be a requirement to work within a wide range of specialties; therefore, this role requires a high degree of flexibility, confidence and self-motivation. The responsibilities of this role will include day to day office admin, supporting the clinical team in the preparation of patient research visits, data input and ensuring robust maintenance of research documentation.About usOur STAR values - Service, Teamwork, Ambition and Respect - are a golden thread running through everything we do. These values serve as a guiding principle, driving us towards our vision of delivering great joined up services to our local community. Whether at home, in the community, or within the hospital, our goal is to empower individuals to lead independent and healthier lives.Job descriptionJob responsibilitiesWork with the lead Research Nurse/OT/AHP to ensure that the Investigator site files are maintained with strict version control according to regulatory requirements. Produce participant/recruitment packs for studies and trials. Ensuring clinical research delivery team haveall the necessary documents to hand for patient clinics in a timely and organised manner. Liaise closely with the research nurses to ensure study visits are booked accurately and according to the visit type stipulated in the research protocol. To assist in the collating all required documents for research project applications in line with the relevant R&I process ensuring required signatures are obtained where necessary. To maintain R&I information resources including notice-boards, information packs and handbooks To assist with the ordering of all stationery and medical supplies for research staff using the appropriateprocurement system. Maintain office filing and creating new study folders To understand and assist with the close-down and archiving of completed research projects in conjunction with other team members or when advised to do so by the Lead R&I Facilitator in line with the current relevant R&I procedure. To maintain confidentiality of all research information. Identify improved ways of working and propose changes to practices, procedures and processed in ownarea of work as well as other areas of work where relevant. Implement any changes to own area of work. To work autonomously, managing own workload effectively and only referring to line manager whennecessary. Able to work with databases in order to assist with the uploading of confidential and sometimes complexdocumentation. Support the preparation all research documents for archiving.Patient Care It is expected any contact with patients will be incidental.Financial Responsibilities The individual may take responsibility for stationary stock ordering.Responsibilities for People or Training It is not expected that this post will be responsible for any people or trainingJob description Job responsibilitiesWork with the lead Research Nurse/OT/AHP to ensure that the Investigator site files are maintained with strict version control according to regulatory requirements. Produce participant/recruitment packs for studies and trials. Ensuring clinical research delivery team haveall the necessary documents to hand for patient clinics in a timely and organised manner. Liaise closely with the research nurses to ensure study visits are booked accurately and according to the visit type stipulated in the research protocol. To assist in the collating all required documents for research project applications in line with the relevant R&I process ensuring required signatures are obtained where necessary. To maintain R&I information resources including notice-boards, information packs and handbooks To assist with the ordering of all stationery and medical supplies for research staff using the appropriateprocurement system. Maintain office filing and creating new study folders To understand and assist with the close-down and archiving of completed research projects in conjunction with other team members or when advised to do so by the Lead R&I Facilitator in line with the current relevant R&I procedure. To maintain confidentiality of all research information. Identify improved ways of working and propose changes to practices, procedures and processed in ownarea of work as well as other areas of work where relevant. Implement any changes to own area of work. To work autonomously, managing own workload effectively and only referring to line manager whennecessary. Able to work with databases in order to assist with the uploading of confidential and sometimes complexdocumentation. Support the preparation all research documents for archiving.Patient Care It is expected any contact with patients will be incidental.Financial Responsibilities The individual may take responsibility for stationary stock ordering.Responsibilities for People or Training It is not expected that this post will be responsible for any people or trainingPerson SpecificationExperienceEssentialAdministrative or clerical experience DesirablePrevious employment within a healthcare setting Clinical Research experience QualificationsEssentialGCSE (A-C Grade) in at least 2 subjects - Including Maths and English (Minimum requirement for all posts)/NVQ Level 2 or equivalent training and experience DesirableEuropean Computer Driving License (or equivalent computer skills qualification) NVQ in Administration Good Clinical Practice training Person Specification ExperienceEssentialAdministrative or clerical experience DesirablePrevious employment within a healthcare setting Clinical Research experience QualificationsEssentialGCSE (A-C Grade) in at least 2 subjects - Including Maths and English (Minimum requirement for all posts)/NVQ Level 2 or equivalent training and experience DesirableEuropean Computer Driving License (or equivalent computer skills qualification) NVQ in Administration Good Clinical Practice training 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. .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. .Employer detailsEmployer nameGreat Western Hospitals NHS Foundation Trust AddressGreat Western HospitalSwindonSN3 6BBEmployer's website #J-18808-Ljbffr
Job Title
Clinical Research Administrator