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- £56k - £72k per annumEstimated...teams to ensure smooth study delivery. Work closely with internal teams and external partners. Help develop and update study documents (e.g., protocols, informed consent forms). Manage third-party vendors, including contracts and budgets. Ensure all study activities...SuggestedRemote jobPermanentWork from homeFlexible hours
- ...with Study Management on identified issues and trends Ensure completeness, accuracy, and compliance of Trial Master File (TMF) documentation Support continuous improvement initiatives and process enhancements within Central Monitoring Participate in vendor selection...SuggestedRemote jobFlexible hours
- £32k - £43k per annumEstimated..., consistent, and risk-mitigating resolutions. ~ Uphold rigorous data integrity by maintaining comprehensive, GDPR-compliant documentation (including investigative notes and final reports) and ensuring the regional ER case tracker is updated weekly with open cases, and...SuggestedFixed-term contractHybrid workingOn-site
£45k - £60k per annum
...team established to oversee delivery of operating model and controls for the Basel 3 Reforms programme. Key Accountabilities: To document the business process controls, IT general controls and Business Application Controls and ensure full syndication and approval from...SuggestedFull-timeInterimOn-siteRemote2 days/week- £46k - £61k per annumEstimated...adherence to study protocols and timely resolution of site-related issues. Assisting in the preparation and review of project related documents in the Investigator Site File and Trial Master File, ensuring all site activities are compliant with GCP and applicable regulations....SuggestedRemote jobFlexible hours
- £44k - £58k per annumEstimated...internal and external stakeholders. * Prepare mission-specific reports, key intelligence insights and Serve as primary client P.O.C. * Document, track, and escalate client feedback to operational teams. * Maintain and update client-facing SOPs, operational documentation and...SuggestedPermanentHybrid workingRemote
- £49k - £66k per annumEstimated...(including mapping specifications) of low to moderate complexity at a minimum. All programs must be developed in accordance with documented procedures and project-specific timelines to generate accurate, complete and consistent outputs. Collaborating with biostatisticians...SuggestedRemote jobFlexible hours
- £42k - £55k per annumEstimated...in safety review meetings and providing expert input on safety-related matters. Contributing to the preparation of safety-related documents for regulatory submissions and responses to regulatory queries. Your Profile: You will bring relevant scientific...SuggestedRemote jobFlexible hours
- £49k - £62k per annumEstimated...meetings and other study related meetings. Provide input into and hold accountability for the development of essential study level documents (i.e., Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant AZ SOPs. Ensure all...SuggestedRemote jobFlexible hours
- £59k - £76k per annumEstimated...Mentoring and guiding team members, fostering a culture of excellence and continuous improvement. Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner. Staying abreast of industry trends and...SuggestedRemote jobFlexible hours
- £34k - £45k per annumEstimated...tech stack. Run full launch cycles from internal testing to early access to GA, including customer enablement through webinars, documentation, and training sessions. Demo your own products to customers and co-sell alongside sales. You’ll be known by name in our...SuggestedRemote jobLive-in
- £69k - £89k per annumEstimated...of innovative treatments and therapies. What you will be doing ~ Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions,...SuggestedRemote jobFlexible hours
- £54k - £71k per annumEstimated...get maximum performance and utility for our cutting-edge products. Responsibilities and Duties Design, implement, test and document OS Kernel and Device Driver software at the highest standard using C/C++/Python programming languages Participate in agile...SuggestedLong-term contractFlexible hours
- £54k - £69k per annumEstimated...actively engaging team members from start to closure Use project management tools for lean execution of a project Analyze and document complex client business requirements and processes; communicate these requirements to appropriate parties Continuously evaluate roadmap...SuggestedRemote jobFlexible hours
- ...onboard applications from different languages/platforms. • As a Kafka SRE you will conduct root cause analysis of production incidents, document for reference and put into place proactive measures to enhance system reliability. Automate routine tasks using scripts or...SuggestedHybrid workingOn-siteImmediate startRemote
- £43k - £55k per annumEstimated...and Heavy Maintenance operation; Administration of the safety occurrences on the Safety reporting system; Preparing reports and documents; Coordinating safety report response amongst production staff. Identify hazards, support risk assessments, and track the...
- £46k - £61k per annumEstimated...Excellence Support day-to-day case handling where needed, while driving efficiency improvements in workflows. Ensure consistent documentation of investigations, decisions, and learnings. Balance operational responsibilities with strategic contributions to the team....Hybrid workingOn-siteRemoteFlexible hours
- £65k - £86k per annumEstimated...compliance teams and other control functions to ensure all development and deployment practices meet regulatory requirements, with proper documentation and auditability in place. Quality Assurance: Line manage QA engineers, manage the QA automation roadmap and work with the Head...Remote jobFlexible hours
- £62k - £79k per annumEstimated...trials Develop and/or oversee the preparation of clinical development plans, study concept sheets, study protocols or regulatory documentation in collaboration with clinical and project team members for assigned indication(s)/products or with external partners for...Remote jobFlexible hours