Date posted
Commute time
Locations
Job types
Salaries
Locations
Locations
Salaries
Date posted
Job types
Locations
Approved Premises Residential Worker Annualised Hours - Guildford
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.
1 exact match is 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.
NEW
These jobs might also interest you
)
Advanced degree in Statistics, Biostatistics or related quantitative discipline (MSc or equivalent) with significant relevant post-graduate experience, in oncology, within the pharmaceutical industry or a clinical research setting. You will lead statistical planning and delivery across clinical programs and contribute to clinical developments plans within oncology. Join us to grow your career, make a real impact on patient-focused R&D, and help unite science, technology and talent to get ahead of disease together. * Provide statistical support to Projects across Oncology pipeline * Lead statistical design, analysis and interpretation for clinical programs across development phases using a wide range of statistical approaches (e.g. Bayesian methodology) * PhD in Statistics, Biostatistics, or closely related field. Please take a copy of the Job Description, as this will not be ...
Advanced degree in Statistics, Biostatistics or related quantitative discipline (MSc or equivalent) with significant relevant post-graduate experience, in oncology, within the pharmaceutical industry or a clinical research setting. You will lead statistical planning and delivery across clinical programs and contribute to clinical developments plans within oncology. Join us to grow your career, make a real impact on patient-focused R&D, and help unite science, technology and talent to get ahead of disease together. * Provide statistical support to Projects across Oncology pipeline * Lead statistical design, analysis and interpretation for clinical programs across development phases using a wide range of statistical approaches (e.g. Bayesian methodology) * PhD in Statistics, Biostatistics, or closely related field. Please take a copy of the Job Description, as this will not be ...
NEW
)
As a Clinical Advisor, you will provide clinical support, training and advice to customers and our business to ensure the correct products are installed that meet individual patient needs. We are looking for a Clinical Advisor to join us on a part-time, permanent basis, covering hospitals within the East London and Northeast London area (Barking, Havering, Redbridge, Homerton). Taking on this engaging role, youll discover that we are dedicated to patient outcomes and are eager to advance clinical environments to achieve this. We work in an advisory capacity and have had huge successes in utilising our equipment and clinical solutions to meet and exceed the needs of both patients and Trusts. - Act as a trusted advisor and provide ongoing bedside training on wards/in the community to help patients use equipment
As a Clinical Advisor, you will provide clinical support, training and advice to customers and our business to ensure the correct products are installed that meet individual patient needs. We are looking for a Clinical Advisor to join us on a part-time, permanent basis, covering hospitals within the East London and Northeast London area (Barking, Havering, Redbridge, Homerton). Taking on this engaging role, youll discover that we are dedicated to patient outcomes and are eager to advance clinical environments to achieve this. We work in an advisory capacity and have had huge successes in utilising our equipment and clinical solutions to meet and exceed the needs of both patients and Trusts. - Act as a trusted advisor and provide ongoing bedside training on wards/in the community to help patients use equipment
)
Medical Administrator/Receptionist London - Harley Street (primary), with travel to other sites (Hatton Garden & Barbican) We are seeking a professional and talented Medical Reception/Administrators to join our client's team and play a crucial role in ensuring the smooth operation of their clinic. * Order office and medical supplies, vaccines, and equipment * Proven experience as a receptionist/administrator in a private healthcare setting (essential) * Familiarity with medical terminology and procedures is an advantage £28,000 - £30,000 - Private healthcare experience is essential for this position. The primary site is located on Harley Street, though travel to other clinic locations (Hatton Garden and Barbican) is required based on rota needs. * Expertly manage doctors' diaries, appointments, and patient requests * Oversee the efficient functioning of the clinic
Medical Administrator/Receptionist London - Harley Street (primary), with travel to other sites (Hatton Garden & Barbican) We are seeking a professional and talented Medical Reception/Administrators to join our client's team and play a crucial role in ensuring the smooth operation of their clinic. * Order office and medical supplies, vaccines, and equipment * Proven experience as a receptionist/administrator in a private healthcare setting (essential) * Familiarity with medical terminology and procedures is an advantage £28,000 - £30,000 - Private healthcare experience is essential for this position. The primary site is located on Harley Street, though travel to other clinic locations (Hatton Garden and Barbican) is required based on rota needs. * Expertly manage doctors' diaries, appointments, and patient requests * Oversee the efficient functioning of the clinic
)
Regional Head of Technology - Electrophysiology and NeuroVascular - EMEA
Regional Head of Technology - Electrophysiology and NeuroVascular - EMEA
Johnson & Johnson
Wokingham, Berkshire
Competitive
The Director, Regional Head of Technology MedTech EP-CNV EMEA consisting of Midsize Markets, Emerging Markets, France, Germany, Spain, Italy, UK is a business strategist and product-minded technology leader who partners closely with the regional MedTech leadership team to shape growth strategies, modernize platforms, and deliver differentiated digital and AI capabilities for customers and patients. * Reports to: VP & Head of Technology and AI (Electrophysiology, Cardio and Neurovascular) * Serve as strategic technology partner to regional senior leaders; jointly identify opportunities, advise on the transformation and application of technology to unlock growth, efficiency, and superior customer/patient experience. This leader serves as the critical point of connection between business strategy and technology execution, developing technology as a competitive advantage for the region and business.
The Director, Regional Head of Technology MedTech EP-CNV EMEA consisting of Midsize Markets, Emerging Markets, France, Germany, Spain, Italy, UK is a business strategist and product-minded technology leader who partners closely with the regional MedTech leadership team to shape growth strategies, modernize platforms, and deliver differentiated digital and AI capabilities for customers and patients. * Reports to: VP & Head of Technology and AI (Electrophysiology, Cardio and Neurovascular) * Serve as strategic technology partner to regional senior leaders; jointly identify opportunities, advise on the transformation and application of technology to unlock growth, efficiency, and superior customer/patient experience. This leader serves as the critical point of connection between business strategy and technology execution, developing technology as a competitive advantage for the region and business.
NEW
)
A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
FEATURED
)
The Medical Monitor 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 Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. * Provide medical management and expertise for clinical trials; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical-related clinical research is preferred.
The Medical Monitor 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 Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. * Provide medical management and expertise for clinical trials; * Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials; * Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical-related clinical research is preferred.
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;
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;
)
Job Title: Head of Health & Social Care The programme includes established communities focused on commercial and procurement issues, interoperability and health data, social care, frontline digitisation and life sciences, and continues to expand into new areas of strategic importance such as femtech. The role is responsible for setting the strategic direction of the programme, growing its impact and commercial performance, and ensuring techUK remains the leading industry voice on how technology can transform health and social care. * Strong understanding of the UK health and social care landscape, including the policy agenda, key stakeholders and the role of technology in transformation. Candidates with experience of: Policy Manager, ecommerce Policy Manager, Policy Adviser, Senior Policy Adviser, Head of Health Programme, ...
Job Title: Head of Health & Social Care The programme includes established communities focused on commercial and procurement issues, interoperability and health data, social care, frontline digitisation and life sciences, and continues to expand into new areas of strategic importance such as femtech. The role is responsible for setting the strategic direction of the programme, growing its impact and commercial performance, and ensuring techUK remains the leading industry voice on how technology can transform health and social care. * Strong understanding of the UK health and social care landscape, including the policy agenda, key stakeholders and the role of technology in transformation. Candidates with experience of: Policy Manager, ecommerce Policy Manager, Policy Adviser, Senior Policy Adviser, Head of Health Programme, ...
PREMIUM
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer to join our Global Clinical Coding & Support team. * Comprehensive manual review of clinical data collected in trials * Development of clinical review guidelines for specific therapeutic areas * General knowledge of clinical trial processes and/or experience working with clinical data * Interface with Data Management team to assure query resolution * Bachelors Degree in Nursing, or more advanced clinical degree - Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - This position will work on a team to accomplish tasks and projects that are instrumental to the companys success.
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer to join our Global Clinical Coding & Support team. * Comprehensive manual review of clinical data collected in trials * Development of clinical review guidelines for specific therapeutic areas * General knowledge of clinical trial processes and/or experience working with clinical data * Interface with Data Management team to assure query resolution * Bachelors Degree in Nursing, or more advanced clinical degree - Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - This position will work on a team to accomplish tasks and projects that are instrumental to the companys success.
)
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
FEATURED
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working 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 ...
Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working 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 ...
Learn more at are searching for the best talent for Manager, Medical Writing, Immunology. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is recruiting for a Manager, Regulatory Medical, Immunology. * If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team. * At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required. Medical Writing * Actively participate in medical writing and cross-functional meetings. * Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the work of other medical writers, external contractors, and document specialists supporting a project. * May represent Medical Writing department in industry standards working groups.
Learn more at are searching for the best talent for Manager, Medical Writing, Immunology. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is recruiting for a Manager, Regulatory Medical, Immunology. * If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team. * At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required. Medical Writing * Actively participate in medical writing and cross-functional meetings. * Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the work of other medical writers, external contractors, and document specialists supporting a project. * May represent Medical Writing department in industry standards working groups.
)
Do you want to have opportunities toparticipateinresearchprojects, special interest groups andform part of a wider occupational therapy networkthat meets regularly for training& development? You will be given responsibility for holding an occupational therapycaseload, with the full support ofyour designated clinical supervisor and site lead, also contributing to staff training and consultationasrequired? * Relevant experienceinproviding occupational therapy services within a similarsetting ispreferrable - Are you looking for an employer who can offer you opportunities for growthand developmentin youroccupational therapy career- All whilst working withina friendly multidisciplinary team?in a rewardingeducationsetting? Do you want to have flexibility and be able to work creatively to deliverspecialist OT assessment and intervention fostering independence within an education setting?
Do you want to have opportunities toparticipateinresearchprojects, special interest groups andform part of a wider occupational therapy networkthat meets regularly for training& development? You will be given responsibility for holding an occupational therapycaseload, with the full support ofyour designated clinical supervisor and site lead, also contributing to staff training and consultationasrequired? * Relevant experienceinproviding occupational therapy services within a similarsetting ispreferrable - Are you looking for an employer who can offer you opportunities for growthand developmentin youroccupational therapy career- All whilst working withina friendly multidisciplinary team?in a rewardingeducationsetting? Do you want to have flexibility and be able to work creatively to deliverspecialist OT assessment and intervention fostering independence within an education setting?
NEW
)
Position: Science Teacher If you are a dedicated Science Teacher looking for a rewarding role, we would be delighted to hear from you. * Plan and deliver engaging and well-structured Science lessons across Key Stages 3 and 4. * Inspire curiosity and enthusiasm for Science while developing students' analytical and investigative skills * Contribute to curriculum development and share best practice within the Science department * Qualified Teacher Status (QTS) - essential * Experience teaching Science in a UK secondary school * Supportive, welcoming and collaborative Science department - Supportive Secondary School in Surrey - This welcoming and well-regarded secondary school is located in Staines and serves a thriving local community. The co-educational school is known for its inclusive ethos, strong pastoral care, and commitment to helping every student achieve their full potential.
Position: Science Teacher If you are a dedicated Science Teacher looking for a rewarding role, we would be delighted to hear from you. * Plan and deliver engaging and well-structured Science lessons across Key Stages 3 and 4. * Inspire curiosity and enthusiasm for Science while developing students' analytical and investigative skills * Contribute to curriculum development and share best practice within the Science department * Qualified Teacher Status (QTS) - essential * Experience teaching Science in a UK secondary school * Supportive, welcoming and collaborative Science department - Supportive Secondary School in Surrey - This welcoming and well-regarded secondary school is located in Staines and serves a thriving local community. The co-educational school is known for its inclusive ethos, strong pastoral care, and commitment to helping every student achieve their full potential.
FEATURED
)
(Aligned to Senior Assessment Researcher / Senior Psychometrician level) We are looking for an experienced researcher to join our English Language Learning division, supporting the delivery and ongoing development of high-stakes English language assessments used globally. About the Role - In this role, youll lead and contribute to research and validation activities that ensure our assessments are robust, reliable, and fit for purpose. Youll work across established products like PTE Academic, as well as new assessment developments, helping to maintain regulatory recognition and support continuous innovation. Our Team - You will be part of the Assessment Research and Validity team , responsible for ensuring Pearsons assessments are psychometrically sound and supported by strong validation evidence. The team works across a range of activities, including test performance monitoring, standards ...
(Aligned to Senior Assessment Researcher / Senior Psychometrician level) We are looking for an experienced researcher to join our English Language Learning division, supporting the delivery and ongoing development of high-stakes English language assessments used globally. About the Role - In this role, youll lead and contribute to research and validation activities that ensure our assessments are robust, reliable, and fit for purpose. Youll work across established products like PTE Academic, as well as new assessment developments, helping to maintain regulatory recognition and support continuous innovation. Our Team - You will be part of the Assessment Research and Validity team , responsible for ensuring Pearsons assessments are psychometrically sound and supported by strong validation evidence. The team works across a range of activities, including test performance monitoring, standards ...
NEW
)
Trusts Fundraising Manager
Trusts Fundraising Manager
Kisharon Langdon
Roe Green Village, North West London (NW9), NW9
GBP 42000.0 - 47000.0 per annum.
Kisharon Langdon has an exciting opportunity for Trusts Fundraising Manager to join their growing Fundraising team in North West London. The Trusts Fundraising Manager plays a key role in securing voluntary income for Kisharon Langdon by leading the development and delivery of a strategic trusts and foundations programme, with responsibility for achieving significant income targets and supporting the organisations long-term growth. To submit your CV for this Trusts Fundraising Manager opportunity click Apply now! - Develop and deliver a clear trusts and foundations strategy to maximise income and support organisational growth - Manage a portfolio of trusts and foundations, leading on cultivation, solicitation and stewardship to secure significant grants and meet agreed income targets - Minimum 2 years proven successful experience in applications to charitable trusts and foundations
Kisharon Langdon has an exciting opportunity for Trusts Fundraising Manager to join their growing Fundraising team in North West London. The Trusts Fundraising Manager plays a key role in securing voluntary income for Kisharon Langdon by leading the development and delivery of a strategic trusts and foundations programme, with responsibility for achieving significant income targets and supporting the organisations long-term growth. To submit your CV for this Trusts Fundraising Manager opportunity click Apply now! - Develop and deliver a clear trusts and foundations strategy to maximise income and support organisational growth - Manage a portfolio of trusts and foundations, leading on cultivation, solicitation and stewardship to secure significant grants and meet agreed income targets - Minimum 2 years proven successful experience in applications to charitable trusts and foundations
PREMIUM
Medpace is currently seeking candidates with Gastrointestinal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working 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 ...
Medpace is currently seeking candidates with Gastrointestinal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working 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 ...
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 ...
)
Head of R&D - Sensing Science
Head of R&D - Sensing Science
KO2 Embedded Recruitment Solutions LTD
Heathway, Dagenham (RM10), RM9 5AQ
£80000 - £90000 per annum
An innovative, venture-backed technology company developing next-generation intelligence and sensing systems is seeking a Head of R&D to lead its sensing strategy and scientific function. * Lead the company's sensing science and R&D strategy * Scientific R&D leadership - You'll work closely with engineering, firmware, software and data science teams to define how sensors are selected, tested, integrated and optimised within commercial products. * Support the development of new sensing products and applications - Location: Dagenham, Essex (2-3 days onsite) Salary: £80,000-£90,000 + benefits - Type: Permanent - Having recently secured oversubscribed seed funding and with commercial products already in market, the business is scaling rapidly across applications including pest control, agriculture, animal health, environmental monitoring and future public health solutions. The Opportunity
An innovative, venture-backed technology company developing next-generation intelligence and sensing systems is seeking a Head of R&D to lead its sensing strategy and scientific function. * Lead the company's sensing science and R&D strategy * Scientific R&D leadership - You'll work closely with engineering, firmware, software and data science teams to define how sensors are selected, tested, integrated and optimised within commercial products. * Support the development of new sensing products and applications - Location: Dagenham, Essex (2-3 days onsite) Salary: £80,000-£90,000 + benefits - Type: Permanent - Having recently secured oversubscribed seed funding and with commercial products already in market, the business is scaling rapidly across applications including pest control, agriculture, animal health, environmental monitoring and future public health solutions. The Opportunity
FEATURED
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in London. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in London. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
The Medical Monitor 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 Monitors to join our dynamic team. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Monitors 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 Monitor 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 Monitors to join our dynamic team. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Monitors 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 ...
Medical Affairs Lead
Medical Affairs Lead
UKPharm Limited
City of London (EC1)
Up to £110,000 per annum bonus and full benefits package
Medical Lead (final signatory) - Pharmaceutical - London - You will have good experienced turning medical evidence into into clear, clinically-sound value narratives, leading medical strategy and being the trusted medical partner for all commercial functions. A fantastic opportunity to enter one of the most buoyant pharmaceutical markets in the UK at present in a consistent state of rapid growth both in turnover and their structure. The role would be office based three days a week in London. They offer a strong package plus bonus in addition to a good peripheral package including such as pension and healthcare.
Medical Lead (final signatory) - Pharmaceutical - London - You will have good experienced turning medical evidence into into clear, clinically-sound value narratives, leading medical strategy and being the trusted medical partner for all commercial functions. A fantastic opportunity to enter one of the most buoyant pharmaceutical markets in the UK at present in a consistent state of rapid growth both in turnover and their structure. The role would be office based three days a week in London. They offer a strong package plus bonus in addition to a good peripheral package including such as pension and healthcare.
)
Functional Assessor
Functional Assessor
Ingeus
East London (E1)
Up to £46813 per annum + 10% bonus and competitive benefits package
As a Functional Assessor with Ingeus, you'll use your clinical reasoning to assess how health conditions impact daily living. Hybrid Working (2 days from home/3 days in the Assessment Centre) If you're a clinician with broad experience across multiple adult conditions and want structured work with predictable hours, this role offers a alternative to traditional practice. If your experience has been focused on a single speciality or limited patient group, this role is unlikely to be the right fit. This is not a hands-on clinical role. It is report-based and requires strong report writing skills and comfort with structured frameworks. The Role * Review medical evidence and complete clinical triage * Use focused questioning and active listening * Produce clear, structured reports to strict standards that enable DWP decision making. What You Need * NMC or HCPC registration with no restrictions
As a Functional Assessor with Ingeus, you'll use your clinical reasoning to assess how health conditions impact daily living. Hybrid Working (2 days from home/3 days in the Assessment Centre) If you're a clinician with broad experience across multiple adult conditions and want structured work with predictable hours, this role offers a alternative to traditional practice. If your experience has been focused on a single speciality or limited patient group, this role is unlikely to be the right fit. This is not a hands-on clinical role. It is report-based and requires strong report writing skills and comfort with structured frameworks. The Role * Review medical evidence and complete clinical triage * Use focused questioning and active listening * Produce clear, structured reports to strict standards that enable DWP decision making. What You Need * NMC or HCPC registration with no restrictions
FEATURED