Assess scientific and technical queries that arise during ARSAC licence application process Analyse and interpret comments made by ARSAC members, where expert opinions may differ, and compare options to provide a resolution Communicate scientific and technical information with a range of healthcare professionals and research trial sponsor organisations Authorise employer and practitioner licences issued under IR(ME)R 2017 on behalf of the Licensing Authorities following completion of quality assurance checks Propose and develop changes to procedures to improve working practices, in conjunction with line manager and in association with various Agencies Use Jira to manage applications according to procedures Use database software to generate reports and provide data analysis for presentation to ARSAC members or external organisations Prepare scientific and technical papers for ARSAC meetings in collaboration with line manager Work with secretariat colleagues to plan ARSAC work programme and meet requirements Identify areas requiring further research and development; co-ordinate and undertake this specialist research work Provide independent expert advice on matters associated with nuclear medicine to service users across the UK Input into radiation protection issues relating to nuclear medicine to promote and improve patient safety in the clinical environment Work with national and international stakeholders to include patients, healthcare professionals, professional bodies associated with nuclear medicine, government bodies, inspectorates for IR(ME)R for the devolved administrations and members of the public on matters pertaining to their field of expertise Work independently on a day to day basisCommunicate the details and outcomes of work through written reports Observe and comply with Data Protection and all other relevant legislation, and UKHSA governance procedures Please see the job description for the full list of duties and responsibilities. Selection Process Details This vacancy will be assessed using a competency-based framework which will assess your qualifications, knowledge and experience and / or skills and abilities outlined in the essential criteria. Stage 1: Application & Sift You will be required to complete an application form. You will be assessed on the listed 9 essential criteria that have been selected from the job description, and this will be in the form of a: Application form (Employer/ Activity history section on the application) (1250 number of words) word Statement of Suitability. This should outline how your skills, experience, and knowledge, provide evidence of your suitability for the role, with reference to the essential criteria. The Application form and Statement of Suitability will be marked together. Longlisting: In the event of a large number of applications we will longlist into 3 piles of: Meets all essential criteria Meets some essential criteria Meets no essential criteria Please note that only those applications meeting all essential criteria will be taken through to shortlisting. Shortlisting: In the event of a large number of applications we will shortlist on: Established and experienced HCPC registered clinical scientist who can provide analysis of practices and advice to enable regulatory compliance and improved clinical practice Up-to-date knowledge and experience of clinical practice in nuclear medicine practice and the associated risks If you are successful at this stage, you will progress to interview and assessment. Please do not exceed 1250 words. We will not consider any words over and above this number. Please note you will not be able to upload your CV. You must complete the application form in as much detail as possible. Please do not email us your CV. Feedback will not be provided at this stage. Stage 2: Interview You will be invited to a remote interview. Knowledge, experience, skills & abilities will be tested at interview. You will be asked to prepare and present an 8-minute presentation at the start of your interview. The subject of this will be sent to you prior to interview. Once this job has closed, the job advert will no longer be available. You may want to save a copy for your records. Eligibility Criteria Open to all external applicants (anyone) from outside the Civil Service (including by definition internal applicants). Location This role is being offered as hybrid working based at our Scientific Campus in Chilton, Oxfordshire. We offer great flexible working opportunities at UKHSA and operate using a hybrid working model where business needs allow. This provides us with greater flexibility about how and where we work, to get the best from our workforce. As a hybrid worker, you will be expected to spend a minimum of 60% of your contractual working hours (approximately 3 days a week pro rata, averaged over a month). Security Clearance Level Requirement Successful candidates for this role must pass an enhanced disclosure and barring security check before they can be appointed. Successful candidates must meet the security requirements before they can be appointed. The level of security needed is Counter-Terrorist Checks. For meaningful National Security Vetting checks to be carried out individuals need to have lived in the UK for a sufficient period of time. You should normally have been resident in the United Kingdom for the last 3 years as the role requires Counter Terrorism Check (CTC) clearance.UK residency less than the outlined periods may not necessarily bar you from gaining national security vetting and applicants should contact the Vacancy Holder / Recruiting Manager listed in the advert for further advice.