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Cancer Research UK
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  • Assistant Shop Manager (Aylesbury)  

    - Aylesbury
    At Cancer Research UK, we exist to beat cancer .We are professionals w... Read More
    At Cancer Research UK, we exist to beat cancer .We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That’s why we’re looking for someone talented, someone who shares our vision, someone like you.We’re looking for a motivated assistant shop manager to join Cancer Research UK’s trading team. You’ll be acting as an ambassador for Cancer Research UK, supporting the shop manager and your team to maximise income through people, resources and stock.In a lively, vibrant working environment, you’ll discover something new every day, whether it’s a new high street trend, a new community network or a talent you never knew you had.You’ll also be surrounded by people who are as dedicated to beating cancer as you are. What will I be doing?Supporting the shop manager to guide, inspire and engage a diverse team of paid staff and volunteers.Support the commercial running of the store including display and merchandising, stock management, maintaining shop standards, store layout, sales and income. Leading by example and providing excellent customer and supporter service. Work alongside the shop manager to achieve targets for donated stock, cash, gift aid, average selling price, sell through and stock processing.Creating relationships with your local community and Cancer Research UK colleagues. Supporting the shop manager in the organisation and delivery of creative fundraising events for your store to achieve fundraising targets. Maintaining compliance with health and safety, safeguarding, security, administration and HR policies.Deputising for the shop manager in their absence.What skills are you looking for?A working knowledge of what makes great customer service.Experience of working in a lively and vibrant environment.Adaptability in changing situations, including being able to work effectively independently. Commercial awareness.The ability to create relationships and communicate well.And ideally supervisor experience, and experience of working in, or an understanding of retail and fashion.[Download the full role profile] What will I gain?Each and every one of our employees contributes to our progress and is supporting our work to beat cancer. We think that’s impressive.In return, we make sure you are supported by a generous benefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well.Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more.Our work – from funding cutting-edge research to developing public policy – will change the world. It’s exciting to be part of our team.How do I apply?We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you quickly, fairly and objectively.Our retail teams cover the needs of their stores by working on a rota basis. Whilst a level of flexibility is needed to meet the needs of the business, we don’t forget that you have a life outside of work too. Owing to the nature of this position, any offer of employment for this role will be subject to a satisfactory basic DBS check.You can learn more about our fantastic retail teams on our website. Read Less
  • At Cancer Research UK, we exist to beat cancer .Join our Health System... Read More
    At Cancer Research UK, we exist to beat cancer .
    Join our Health Systems Engagement (HSE) Team and help turn evidence into action.We work at the heart of health systems across the UK, driving the adoption of innovative solutions and reducing cancer inequalities through education, engagement, and impactful programmes. As a Health Programmes Administrator, you’ll play a vital role in supporting our managers and senior leaders, ensuring smooth delivery of projects and operations. From coordinating key activities and managing relationships to handling financial processes and leading small-scale projects, your work will help us make a real difference.What will I be doing?Provide operational, administrative, and project support to deliver products and programmes aligned with the HSE strategy.Take ownership of specific tasks that enable successful delivery of team objectives, such as organising engagement events, managing meetings, and coordinating reporting on designated work packages.Oversee day-to-day administrative and financial processes, including procurement, liaison with funding recipients, and travel or accommodation bookings.Manage key communication processes, ensuring HSE priorities, activities, and successes are shared effectively through newsletters and stakeholder updates.Support the team in using the CRUK customer relationship management system (Salesforce) for relationship management and reporting.Assist with senior and external meetings by preparing papers, taking high-quality minutes, and tracking actions.Lead small-scale projects within the HSE portfolio, with guidance from project and programme managers.Identify opportunities to improve operational processes and keep the team informed of organisational changes.Support governance and oversight activities, including KPI and budget reporting, risk and issue logging, and secretariat functions.Build and maintain relationships with internal and external contacts to ensure smooth delivery of tasks.What are we looking for?Strong organisational skills and experience in administrative support.Awareness of project management principles.Familiarity with Salesforce or other CRM systems.Ability to work with procurement and financial systems.Excellent prioritisation skills and ability to work independently and collaboratively.Proficiency in Microsoft Office and online tools.Confident communicator with experience liaising with external stakeholders or suppliers.Proactive approach to adding value and supporting team objectives.Understanding of data protection principles.Our organisation values are designed to guide all that we do.Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaborativelyWe’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.What will I gain?We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.You can explore our benefits by visiting our careers web page.Additional informationFor more Information on our work and careers, follow us on: LinkedIn, Facebook, Instagram, X and YouTube.Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen. Please contact or 020 3469 8400 as soon as possible. Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks. Read Less
  • Retail Assistant Manager (Surbiton)  

    - Surbiton
    At Cancer Research UK, we exist to beat cancer .​​​We are professional... Read More
    At Cancer Research UK, we exist to beat cancer .​​​We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That’s why we’re looking for someone talented, someone who shares our vision, someone like you.​We’re looking for a motivatedassistantshopmanager to join Cancer Research UK’s trading team. You’ll be acting as an ambassador for Cancer Research UK,supporting the shop managerand your team to maximise income through people, resources and stock. You’ll also be surrounded by people who are as dedicated to beating cancer as you are.What will I be doing?Supporting theshop manager to guide, inspireand engageadiverseteam of paid staff and volunteers. Support thecommercial running ofthestoreincluding display and merchandising, stock management, maintaining shop standards, store layout, sales and income.Leading by example and providing excellent customer and supporter service. Work alongside the shop manager to achieve targets for donated stock, cash, gift aid, average selling price, sell through and stock processing. Creating relationships with your local community and Cancer Research UK colleagues. Supporting the shop manager in the organisationanddelivery ofcreative fundraising events for your store to achieve fundraising targets. Maintaining compliance with health and safety, safeguarding, security, administration and HR policies.Deputising for the shop manager in their absence. There will be a varied amount of manual handling and physical activity required within the day-to-day duties of the role.Whatare you looking for?Aworking knowledge ofwhat makesgreatcustomer service.Experience ofworking in a lively and vibrant environment.Adaptability in changing situations, including being able to work effectively independently.Commercial awareness. The ability to createrelationships and communicate well. Flexibility, our retail teams cover the needs of their stores by working on a rota basis. Whilst a level of flexibility is needed to meet the needs of the business, we don’t forget that you have a life outside of work too. [Download the full role profile]What will I gain?We make sure you are supported by a generoussalary andbenefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well. Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more.Our retail teams also have access to confidential wellbeing support from the Retail Trust.For the full job description and more information about working with us please contactHow do I apply?We operate an anonymised shortlisting processin our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess youquickly,fairly and objectively. Owing to the nature of this position, any offer of employment for this role will be subject to a satisfactory basic DBS check. Read Less
  • At Cancer Research UK, we exist to beat cancer .​​​We are professional... Read More
    At Cancer Research UK, we exist to beat cancer .​​​We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That’s why we’re looking for someone talented, someone who wants to develop their skills, someone like you. ​We’re looking for a proactive stock processor to join Cancer Research UK’s trading team. You’ll be acting as an ambassador for Cancer Research UK, taking care of pre-loved itemsand getting them ready for their new home. You’ll also be surrounded by people who are as dedicated to beating cancer as you are.What will I be doing?Processing and looking after new and donated stock. This includes keeping on top of stock rotation and replenishment, pricing, steaming and tagging.Assisting the store team in achieving sales and fundraising targets.Supporting the training of colleagues and volunteers in stock processing. Ensuring standards of safeguarding, compliance, security and health and safety are followed.Using your customer service skills to make sure our customers and supporters feel welcome and appreciated.There will be a varied amount of manual handling and physical activity required within the day-to-day duties of the role.What are you looking for?Experience working in a busy customer-facing environment.Adaptability to changing situations.A proactive mindset.The ability to manage your own workload and work independently and as part of a team.A positive approach to building relationships with community members.Flexibility, our retail teams cover the needs of their stores by working on a rota basis. Whilst a level of flexibility is needed to meet the needs of the business, we don’t forget that you have a life outside of work too. [Download the full role profile]What will I gain?We make sure you are supported by a generous benefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well. Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more.Our retail teams also have access to confidential wellbeing support from the Retail Trust.How do I apply?We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you quickly, fairly and objectively. Owing to the nature of this position, any offer of employment for this role will be subject to a satisfactory basic DBS check. Read Less
  • Regulatory Medical Writer  

    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK... Read More
    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK Centre for Drug Development (CDD) is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in.As a Medical Writer you’ll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD’s early phase oncology trials. As well as acting as lead author on your assigned projects and performing quality control review of documents produced by other Medical Writers, you will be fully embedded within a multidisciplinary, cross functional project team along with other CDD departments. Collaboration is essential, as well as the ability to work strategically within an evolving environment.Unfortunately, this role is not suitable for anyone who only has experience in medical writing for pharmacovigilance or medical devices or anyone who only has medical writing experience within science comms. You must come with strong knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results. This is a great opportunity for a current Regulatory Medical Writer looking to move into a more purpose driven environment or to gain valuable experience withing phase 1 oncology trials. Or you could be a Medical Writing Associate ready to take that next step.What will I be doing?Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines, and participating in the preparation and review of summary clinical trial results and other disclosures as required.Managing the scheduling, preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.Liaising with the project team to complete project-specific tasks including review of protocols, Trial Master Files, data (including expert reports), and analytical plans.What are you looking for?Proven experience in medical / medical sciences writing. This should include significant experience in regulatory medical writing or a mix of experience in regulatory medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.Science graduate or equivalent experience of scientific writing.Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.Excellent proofreading skills and attention to detail.Confident communication skills and able to foster strong working relationships both internally and externally.Project Management skillsExperience within early phase oncology trials is desirable but not essential (*Please do still apply even if you don’t have this*)Experience within AI medical writing tools is beneficialOur organisation values are designed to guide all that we do.Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaborativelyWe’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience we’d still love to hear from you.What will I gain?We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.You can explore our benefits by visiting our careers web page.How do I apply?We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. Read Less
  • Regulatory Medical Writer  

    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK... Read More
    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK Centre for Drug Development (CDD) is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in.As a Medical Writer you’ll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD’s early phase oncology trials. As well as acting as lead author on your assigned projects and performing quality control review of documents produced by other Medical Writers, you will be fully embedded within a multidisciplinary, cross functional project team along with other CDD departments. Collaboration is essential, as well as the ability to work strategically within an evolving environment.Unfortunately, this role is not suitable for anyone who only has experience in medical writing for pharmacovigilance or medical devices or anyone who only has medical writing experience within science comms. You must come with strong knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results. This is a great opportunity for a current Regulatory Medical Writer looking to move into a more purpose driven environment or to gain valuable experience withing phase 1 oncology trials. Or you could be a Medical Writing Associate ready to take that next step.What will I be doing?Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines, and participating in the preparation and review of summary clinical trial results and other disclosures as required.Managing the scheduling, preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.Liaising with the project team to complete project-specific tasks including review of protocols, Trial Master Files, data (including expert reports), and analytical plans.What are you looking for?Proven experience in medical / medical sciences writing. This should include significant experience in regulatory medical writing or a mix of experience in regulatory medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.Science graduate or equivalent experience of scientific writing.Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.Excellent proofreading skills and attention to detail.Confident communication skills and able to foster strong working relationships both internally and externally.Project Management skillsExperience within early phase oncology trials is desirable but not essential (*Please do still apply even if you don’t have this*)Experience within AI medical writing tools is beneficialOur organisation values are designed to guide all that we do.Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaborativelyWe’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience we’d still love to hear from you.What will I gain?We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.You can explore our benefits by visiting our careers web page.How do I apply?We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. Read Less
  • Regulatory Medical Writer  

    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK... Read More
    At Cancer Research UK, we exist to beat cancer .The Cancer Research UK Centre for Drug Development (CDD) is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in.As a Medical Writer you’ll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD’s early phase oncology trials. As well as acting as lead author on your assigned projects and performing quality control review of documents produced by other Medical Writers, you will be fully embedded within a multidisciplinary, cross functional project team along with other CDD departments. Collaboration is essential, as well as the ability to work strategically within an evolving environment.Unfortunately, this role is not suitable for anyone who only has experience in medical writing for pharmacovigilance or medical devices or anyone who only has medical writing experience within science comms. You must come with strong knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results. This is a great opportunity for a current Regulatory Medical Writer looking to move into a more purpose driven environment or to gain valuable experience withing phase 1 oncology trials. Or you could be a Medical Writing Associate ready to take that next step.What will I be doing?Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines, and participating in the preparation and review of summary clinical trial results and other disclosures as required.Managing the scheduling, preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.Liaising with the project team to complete project-specific tasks including review of protocols, Trial Master Files, data (including expert reports), and analytical plans.What are you looking for?Proven experience in medical / medical sciences writing. This should include significant experience in regulatory medical writing or a mix of experience in regulatory medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.Science graduate or equivalent experience of scientific writing.Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.Excellent proofreading skills and attention to detail.Confident communication skills and able to foster strong working relationships both internally and externally.Project Management skillsExperience within early phase oncology trials is desirable but not essential (*Please do still apply even if you don’t have this*)Experience within AI medical writing tools is beneficialOur organisation values are designed to guide all that we do.Bold: Act with ambition, courage and determination Credible: Act with rigour and professionalism Human: Act to have a positive impact on people Together: Act inclusively and collaborativelyWe’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience we’d still love to hear from you.What will I gain?We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance, take positive steps in your career and achieve your personal wellbeing goals.You can explore our benefits by visiting our careers web page.How do I apply?We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively. Read Less

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