Date posted
Commute time
Locations
Type of Company
Job types
Salaries
Locations
Filters
Locations
Salaries
Date posted
Type of Company
Job types
Locations
1 Part Time API job in Maidenhead + 30 miles
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
)
You possess deep domain knowledge in language models and generative AI model architectures, including fine-tuning techniques beyond API-level implementation.
You possess deep domain knowledge in language models and generative AI model architectures, including fine-tuning techniques beyond API-level implementation.
These jobs might also interest you
)
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
)
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 ...
NEW
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.
Medpace is currently seeking candidates with 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 clinical project ...
Medpace is currently seeking candidates with 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 clinical project ...
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 ...
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.
Medpace is currently seeking candidates with 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 clinical project ...
Medpace is currently seeking candidates with 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 clinical project ...
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 ...
)
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.
NEW
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.
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 ...
Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical-related clinical research is preferred. Medpace is a full-service clinical contract research organization (CRO). 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. * Provide medical management and expertise for clinical trials; * Manage safety issues in clinical trials and work closely with associates in ...
Prior clinical trial research experience preferred; and * Previous experience in pharmaceutical-related clinical research is preferred. Medpace is a full-service clinical contract research organization (CRO). 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. * Provide medical management and expertise for clinical trials; * Manage safety issues in clinical trials and work closely with associates in ...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, 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
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, 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
)
This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
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.
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our UK team and to be based at our growing UK office in London. * Manage Clinical Safety activities and multiple large programs * Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality; * Provide safety review of clinical study documents, including protocols, study reports; and marketing application components. * Bachelors degree or equivalent and clinical safety experience, including project management and ideally line management experience; * Previous experience of managing clinical safety activities for multiple programmes; * Comprehensive knowledge of global clinical safety regulatory requirements; This position plays a key role in the pharmacovigilance process at Medpace.
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our UK team and to be based at our growing UK office in London. * Manage Clinical Safety activities and multiple large programs * Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality; * Provide safety review of clinical study documents, including protocols, study reports; and marketing application components. * Bachelors degree or equivalent and clinical safety experience, including project management and ideally line management experience; * Previous experience of managing clinical safety activities for multiple programmes; * Comprehensive knowledge of global clinical safety regulatory requirements; This position plays a key role in the pharmacovigilance process at Medpace.
We are seeking Advanced Nurse Practitioners/ Clinical Nurse Specialists with endocrine experience who are interested in being at the forefront of new treatments for patients with endocrine disease. * Significant experience as a clinical nurse practitioner or nurse consultant within endocrinology; This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in clinical research is preferred. * Develop and implement disease-specific and clinical education for internal teams * Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team * Attend pre-study and study-related meetings with project teams, providing clinical expertise
We are seeking Advanced Nurse Practitioners/ Clinical Nurse Specialists with endocrine experience who are interested in being at the forefront of new treatments for patients with endocrine disease. * Significant experience as a clinical nurse practitioner or nurse consultant within endocrinology; This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in clinical research is preferred. * Develop and implement disease-specific and clinical education for internal teams * Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team * Attend pre-study and study-related meetings with project teams, providing clinical expertise
)
This is a fantastic role for an established teacher or current middle leader looking to step into a Head of Computer Science position, or an experienced Head of Computer Science seeking a new challenge in a dynamic and well-supported school environment in Westminster. As Head of Computer Science, you will lead the department and drive high standards of teaching, learning, and student outcomes. * Experience in a leadership role or readiness to step into a Head of Computer Science position - An exciting opportunity has arisen for an ambitious and experienced Computer Science Teacher to lead a growing department in a well-regarded secondary school in Westminster, Central London. * Chance to shape and develop a forward-thinking Computer Science curriculum * Leading and managing the Computer Science department * A qualified teacher with strong subject knowledge in Computer Science
This is a fantastic role for an established teacher or current middle leader looking to step into a Head of Computer Science position, or an experienced Head of Computer Science seeking a new challenge in a dynamic and well-supported school environment in Westminster. As Head of Computer Science, you will lead the department and drive high standards of teaching, learning, and student outcomes. * Experience in a leadership role or readiness to step into a Head of Computer Science position - An exciting opportunity has arisen for an ambitious and experienced Computer Science Teacher to lead a growing department in a well-regarded secondary school in Westminster, Central London. * Chance to shape and develop a forward-thinking Computer Science curriculum * Leading and managing the Computer Science department * A qualified teacher with strong subject knowledge in Computer Science
FEATURED
)
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
We are seeking an Oncologist - Solid Tumor Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. 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. 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;
We are seeking an Oncologist - Solid Tumor Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. 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. 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;
)
This Science Academic Mentor opportunity in Lewisham from September 2026 is ideal for a graduate eager to support pupils across Biology, Chemistry and Physics within a structured secondary school environment. This Science Academic Mentor role is based within a secondary school currently focused on strengthening outcomes, behaviour and curriculum consistency following its transition into. The successful Science Academic Mentor will support pupils through classroom learning, small-group interventions and targeted revision sessions. This Science Academic Mentor role would particularly suit aspiring Science Teachers looking to build strong experience within a secondary school setting. If you are a Science graduate looking for a Science Academic Mentor role that provides meaningful classroom experience and progression, this is an excellent Lewisham opportunity from September 2026.
This Science Academic Mentor opportunity in Lewisham from September 2026 is ideal for a graduate eager to support pupils across Biology, Chemistry and Physics within a structured secondary school environment. This Science Academic Mentor role is based within a secondary school currently focused on strengthening outcomes, behaviour and curriculum consistency following its transition into. The successful Science Academic Mentor will support pupils through classroom learning, small-group interventions and targeted revision sessions. This Science Academic Mentor role would particularly suit aspiring Science Teachers looking to build strong experience within a secondary school setting. If you are a Science graduate looking for a Science Academic Mentor role that provides meaningful classroom experience and progression, this is an excellent Lewisham opportunity from September 2026.
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.
We are seeking Advanced Nurse Practitioners/ Clinical Nurse Specialists with cardiology experience who are interested in being at the forefront of new treatments for patients with cardiovascular disease. * Significant experience as a clinical nurse practitioner or nurse consultant within cardiology; This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in clinical research is preferred. * Develop and implement disease-specific and clinical education for internal teams * Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team * Attend pre-study and study-related meetings with project teams, providing clinical expertise
We are seeking Advanced Nurse Practitioners/ Clinical Nurse Specialists with cardiology experience who are interested in being at the forefront of new treatments for patients with cardiovascular disease. * Significant experience as a clinical nurse practitioner or nurse consultant within cardiology; This role will work side by side with our physicians, serving as clinical expert, to support our project teams in clinical research studies (no direct patient care). Experience in clinical research is preferred. * Develop and implement disease-specific and clinical education for internal teams * Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team * Attend pre-study and study-related meetings with project teams, providing clinical expertise