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      1 Contract API job in Maidenhead + 30 miles

      Approved Premises Residential Worker Annualised Hours - Guildford

      THE HOME OFFICE
      Guildford, Surrey
      £20,001 - £40,000 a year
      Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
      Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
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      2 exact matches jobs are outside your preferred location

      Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
      Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
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      NEW

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      You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
      You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
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      NEWPREMIUM
      R1602299 : Director, Global Clinical Physician The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities. Working with Us - Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
      R1602299 : Director, Global Clinical Physician The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities. Working with Us - Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
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      NEW
      We are seeking a Gastroenterologist / Hepatologist to join our dynamic team. Job Summary - The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Responsibilities * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
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      We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
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      Head of Technology Change Delivery

      Hays
      Leatherhead (KT22)
      £120000.0 - £140000.0 per annum + £140,000
      We are supporting a highly regarded, large-scale organisation within the built environment to appoint a Head of Technology Change Delivery into their Group Technology & Data function. This is a senior leadership appointment, offering the opportunity to operate at enterprise level, taking full accountability for the delivery of a complex portfolio of technology-enabled change initiatives. The successful candidate will bring a proven track record of leading large-scale, business-critical technology change programmes, working in close partnership with senior stakeholders to deliver outcomes that genuinely enable and transform the wider organisation. As a key member of the Technology & Data Leadership Team, you will play a central role in driving forward delivery of excellence across the function. The successful individual will also take ownership of financial governance ...
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      As the Life Sciences Project Manager / Benefits Manager, you will work with colleagues across UKRI to help deliver strategic government and societal priorities through the UKRI Life Sciences programme. To support the effective management, delivery, and coordination of the UKRI Life Sciences Industrial Strategy programme. You will play a key role in programme and project governance, ensuring that intended benefits and outcomes are successfully achieved. * Coordinating and delivering the relevant programmes various projects, dependencies (internal and external), key milestones, risks, governance, financial management, and benefits planning * Developing project specific benefits realisation plans to ensure realisation of benefits for programmes through planning and designing and ensuring that project outputs meet programme requirements.
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      Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
      Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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      Clinical Project Manager

      Pro Contract Jobs Ltd
      London
      From £53,000 to £65,000 per annum fixed-term
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      Establish and grow an internal AI Champions network and communities of practice to spread knowledge, share success stories and embed grassroots enthusiasm for AI. * Act as a visible AI champion, engaging employees and managers, addressing concerns, demonstrating tools in action and supporting local champions. * Drive organisation-wide AI uptake through a people-centred adoption programme, building confidence, responsible use and an AI-enabled culture that improves productivity and ways of working. * Hands-on experience delivering digital solutions, ideally AI-powered or automation-based, from concept through deployment and adoption. * Design and run a comprehensive AI training curriculum for all staff levels, building practical skills, digital confidence and safe, effective use of AI tools. * Lead quick-win delivery of lightweight AI tools embedded in local workflows, ensuring ...
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      FEATURED

      Director of Governance, Risk and Assurance

      Victim Support
      The City, City of London (EC2), EC2A 4BQ
      Up to £83000.00 per annum
      The Director of Governance, Risk and Assurance is a member of the Senior Leadership Team, holding strategic accountability for governance, risk, assurance and quality across the organisation. This newly established role offers a unique opportunity to shape and strengthen organisational governance, risk and assurance frameworks across a national charity delivering vital services to victims of crime. As Director, you will provide strategic leadership across governance, risk management, compliance and quality assurance, ensuring that the organisation operates safely, effectively and in line with its statutory and regulatory responsibilities. This is an exciting new role that will provide leadership as Victim Support grows, ensuring excellent governance, risk management and assurance across the organisation. If you are passionate about good governance and are looking to lead ...
      The Director of Governance, Risk and Assurance is a member of the Senior Leadership Team, holding strategic accountability for governance, risk, assurance and quality across the organisation. This newly established role offers a unique opportunity to shape and strengthen organisational governance, risk and assurance frameworks across a national charity delivering vital services to victims of crime. As Director, you will provide strategic leadership across governance, risk management, compliance and quality assurance, ensuring that the organisation operates safely, effectively and in line with its statutory and regulatory responsibilities. This is an exciting new role that will provide leadership as Victim Support grows, ensuring excellent governance, risk management and assurance across the organisation. If you are passionate about good governance and are looking to lead ...
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      NEWPREMIUM
      The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
      The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
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      NEW
      The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
      The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
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      Frequently Asked Questions

      How many contract API jobs are there in Maidenhead?
      There are 1 contract API jobs within 30 miles of Maidenhead available on EmedCareers right now.

      What other similar jobs are there to contract API jobs in Maidenhead?
      As well as contract API jobs in Maidenhead, you can find contract Science, Data Science, Database, amongst many others.