{"id":1899800,"url":"https://alion.io/job/qureight-clinical-site-manager","title":"Clinical Site Manager","company":{"id":691224,"name":"Qureight","domain":"qureight.com","url":"https://alion.io/company/qureight","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workable","truth_index":null},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":null,"employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Cambridge, United Kingdom","London, United Kingdom"],"countries":["GB"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":43000,"max_usd":90000,"period":"year","method":"role_country_seniority_unknown","sample_n":875},"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"ISO 27001","optional":false},{"name":"21 CFR Part 11","optional":true},{"name":"ISO 13485","optional":true},{"name":"Machine Learning","optional":true}],"status":"live","first_seen_at":"2026-10-14T14:52:41Z","employer_posted_date":"2026-10-14","last_verified_at":"2026-10-29T05:26:30Z","board_verified":true,"closed_at":null,"days_open":14,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":14},"description":"About us\nQureight’s mission is to accelerate clinical trials and ensure breakthroughs in lung and heart disease reach patients without delay. Our AI-powered data and imaging curation platform enables the analysis of clinical imaging and other healthcare data, helping our customers bring treatments to market, faster.\nWe’re looking for talented people who want their work to matter. With offices in Cambridge and London, you’ll join our multidisciplinary team of clinicians, scientists, and engineers. What unites us is our open culture, continuous learning mindset, and a shared mission to help biopharma run faster, smarter trials.\nAbout the role\nThe Clinical Site Manager is responsible for managing clinical trial sites from site qualification to site management, including aspects of data management, image QC and query management, as part of the delivery of Qureight’s imaging CRO services. They ideally have experience in coordinating and managing clinical study sites globally or experience in a clinical trial setting generally.\nA positive and can-do attitude, alongside an understanding of clinical study quality and regulatory standards is essential to the role.\nYou will be responsible for working with...\nConduct Qureight site qualification activities, including site evaluation, training and scanner qualification, to ensure timely onboarding of priority clinical study sites. \nProvide proactive and effective site facing communications to support clinical trial sites in completing site qualification activities before planned activation dates.\nBe responsible for designated site management activities post site qualification including query management. \nBe responsible for raising data queries with site staff and managing them through to completion, in collaboration with data management colleagues.\nBe the point of contact for assigned clinical sites and know when to escalate for guidance and support. \nRespond to and resolve inbound support requests in a timely and efficient manner in line with SOPs. \nCommunicate with all stakeholders in a professional and timely manner. \nTrack and report project and site milestones and maintain relevant internal systems with project specific information. \nWhen necessary, support image check (QC) processes for assigned projects, completing timely and accurate QC in line with SOPs. \nLearn about and develop expertise in CT\nStep up to coordinate all site onboarding activities as site qualification lead for assigned projects as necessary.\nMaintain essential site facing documents, updating and sharing as needed. \nTake part in clinical project kick-off meetings where appropriate. \nConduct work in accordance with Good Clinical Practice (GCP) guidelines and all relevant regulations, including ISO27001 standards and data privacy regulations. \nBe part of driving continuous improvement and operational efficiency by highlightling where improvements could be made.\nBuild strong relationships with all stakeholders (at site, with sponsors, with customers and within Qureight) maintaining transparent and consistent communication throughout. \nSupport general Clinical Operations activities as needed. \nRequirements\nWhat we need:\nDemonstrable experience in clinical trial site management \nDemonstrated experience with clinical imaging, e.g. CT or MRI is desirable but not essential.\nStrong organisational and time management skills with ability to prioritise tasks effectively. \nDemonstrated ability to cultivate and maintain key stakeholder relationships, both internally and externally. \nKnowledge of ICH Good Clinical Practice (GCP) with evidence of recent training. \nExperience working within a Quality Management System (QMS), e.g., ISO 9001, ISO 13485 is desirable. \nKnowledge of relevant regulatory, compliance and industry standards, e.g. 21 CFR Part 11, is desirable. \nStrong interpersonal skills with a high proficiency in written and verbal communications. \nTrack record of working effectively and problem solving in a highly technical and innovative environment, demonstrating a good attention to detail. \nEvidence of a can-do attitude with a tenacity and drive to achieve objectives. \nEven better if you have...\nA relevant degree, for example in life sciences, is desirable but not essential.\nBenefits\nWhat can you expect from us\nA comprehensive benefits package that includes an annual bonus plan, private medical insurance, life insurance, cycle-to-work scheme, and a contributory pension scheme \nEquity, so that our team can share in the long-term success of Qureight\n28 days’ holiday allowance, 25 days’ annual leave and 3 additional company days between Christmas and New Year, plus bank holidays and enhanced family leave\nA diverse work environment that brings together experts in many fields, including software engineering, DevOps, data science, machine learning, quality assurance, regulatory affairs, and clinical operations.\nHow to apply\nPlease upload a CV and covering letter by clicking 'Apply Now'. Your covering letter should explain why you are applying for the job and what skills and experience you can bring to the role. We review CVs as we receive them and interview as soon as we have applications that look like a good match (usually within one week). We do not use closing dates. So, please apply as soon as possible to avoid missing out on this role.\nWe advertised this role on 5th October 2026.Previous applicants for this role need not apply.\nIf you have any queries, please contact . Everyone is welcome at Qureight. We are an equal opportunities employer and encourage applications from all suitably qualified candidates regardless of age, disability, ethnicity, sex, gender reassignment, religion or belief, sexual orientation, marriage and civil partnership, or pregnancy and maternity.\nWomen and other underrepresented groups may be less likely to apply for a role unless they meet all or nearly all of the requirements. If this applies to you, we still encourage you to apply - you may be a great fit, even if you don’t meet every qualification. We’d love to hear from you.\nIf you require any adjustments to the application or selection process, please let us know. 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