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      2 Contract API jobs in South East + 30 miles

      GAIN Customer Science - Tracking Delivery Manager

      THIS IS GAIN LTD
      London
      Competitive
      Google Measurement Protocol & other server-side API technologies.
      Google Measurement Protocol & other server-side API technologies.
      Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
      Overview of the job - The job holder will work as part of a team providing 24 hour cover at an Approved Premises (AP) including security and monitoring services. The job holder will undertake a full range of work with the offender whilst resident at the Approved Premises. This will include; providing support in contributing to the risk management and sentence plan objectives and reporting any significant changes relating to risk and/or re-offending to any non-compliance within agreed enforcement procedures to ensure that offenders resident at an AP and the fabric of it are kept safe and secure throughout their shift. Summary - The job holder will assist in the well-being and supervision of residents, maintaining discipline, adnce to AP rules, licence conditions, sentence plan objectives specific to residency in the Approved Premises and court orders.
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      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.
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      Clinical Project Manager

      Pro Contract Jobs Ltd
      London
      From £53,000 to £65,000 per annum fixed-term
      The Project Manager will be responsible for the operational development, conduct, oversight, and completion of clinical trial research projects. The Project Manager will join the Project Operations team. You will be the main contact as the trial Project Manager, delivering a cardiovascular trial involving patients with hypertension. You will be responsible for all aspects of project management, including the operational development, conduct, oversight, and completion of clinical trial research projects. Excellent stakeholder management, problem-solving skills, and adherence to Good Clinical Practice principles, ethical and regulatory requirements, and applicable Standard Operating Procedures are essential. Project management training course. Excellent knowledge of research and project management principles, ICH/GCP, ethical and regulatory requirements.
      The Project Manager will be responsible for the operational development, conduct, oversight, and completion of clinical trial research projects. The Project Manager will join the Project Operations team. You will be the main contact as the trial Project Manager, delivering a cardiovascular trial involving patients with hypertension. You will be responsible for all aspects of project management, including the operational development, conduct, oversight, and completion of clinical trial research projects. Excellent stakeholder management, problem-solving skills, and adherence to Good Clinical Practice principles, ethical and regulatory requirements, and applicable Standard Operating Procedures are essential. Project management training course. Excellent knowledge of research and project management principles, ICH/GCP, ethical and regulatory requirements.
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      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.
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      R1602299 : Director, Global Clinical Physician The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities. Working with Us - Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
      R1602299 : Director, Global Clinical Physician The Clinical Trial Physician serves as a primary source of medical accountability and oversight for multiple clinical trials, and manages Phase 1 Phase 3 studies, with demonstrated decision making capabilities. Working with Us - Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
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      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 ...
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      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;
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      Our Beauty & Wellness team is seeking a Insight Manager who will actively support the team in building relationships with our clients, providing them with value-added insights and driving revenue within our accounts, as well as having their own account base. * Insight Manager actively support the team in building relationships with our clients (expanding and enhancing our servicing to clients and actively contributing to increase their satisfaction), providing them with value-added insights and driving revenue within our accounts. * A desire for consumer behaviour/purchasing journey, marketing, advertisement, and the economy is a must and preferable within the world of Beauty & Wellness & /Or to put in content of Beauty & Wellness * Enthusiastic and innovative person with a real passion & knowledge for the Beauty & Wellness industry.
      Our Beauty & Wellness team is seeking a Insight Manager who will actively support the team in building relationships with our clients, providing them with value-added insights and driving revenue within our accounts, as well as having their own account base. * Insight Manager actively support the team in building relationships with our clients (expanding and enhancing our servicing to clients and actively contributing to increase their satisfaction), providing them with value-added insights and driving revenue within our accounts. * A desire for consumer behaviour/purchasing journey, marketing, advertisement, and the economy is a must and preferable within the world of Beauty & Wellness & /Or to put in content of Beauty & Wellness * Enthusiastic and innovative person with a real passion & knowledge for the Beauty & Wellness industry.
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      We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
      We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
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      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 ...
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      NEW
      Medpace is currently seeking candidates with Bachelor of Medicine, Bachelor of Surgery qualification for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. A fantastic opportunity for recent junior doctors to enter the clinical research industry in an operations role, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. 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 ...
      Medpace is currently seeking candidates with Bachelor of Medicine, Bachelor of Surgery qualification for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team. A fantastic opportunity for recent junior doctors to enter the clinical research industry in an operations role, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. 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 ...
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      NEW
      As a Qualified Nursery Practitioner, you’ll be providing high-quality care within a nursery setting across the local area. Join Nurseplus as a Qualified Nursery Practitioner – Make a Difference Every Day - As a Nursery Practitioner with Nurseplus, you’ll play a key role in delivering high-quality early years care and education. * Assisting in the daily care, supervision, and wellbeing of children within the nursery setting. * Providing guidance and support to fellow team members, helping to lead by example and ensure best practice across the nursery. At Nurseplus, every shift you work is an opportunity to make a real difference in the lives of those in need. You will be required to provide day-to-day cover for short or longer-term placements, supporting children's development, ensuring their safety, and helping them learn through play.
      As a Qualified Nursery Practitioner, you’ll be providing high-quality care within a nursery setting across the local area. Join Nurseplus as a Qualified Nursery Practitioner – Make a Difference Every Day - As a Nursery Practitioner with Nurseplus, you’ll play a key role in delivering high-quality early years care and education. * Assisting in the daily care, supervision, and wellbeing of children within the nursery setting. * Providing guidance and support to fellow team members, helping to lead by example and ensure best practice across the nursery. At Nurseplus, every shift you work is an opportunity to make a real difference in the lives of those in need. You will be required to provide day-to-day cover for short or longer-term placements, supporting children's development, ensuring their safety, and helping them learn through play.
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      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 ...
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      We are seeking an Dermatologist - 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 Dermatologist - 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;
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      Job Title: Business Development Manager (Healthcare) My clients seeking a highly motivated and results-driven Business Development Manager to join their team at their head office in Dartford. * Performance Reporting: Prepare and present regular, insightful reports on pipeline health, lead generation efforts, sales performance, and overall business development progress to senior management. * Strategic Development: Design, implement, and execute comprehensive business development plans aimed at achieving and exceeding company revenue targets and growth objectives. * Experience: Minimum of 5 years of proven business development or sales experience, specifically within the hard facilities management (FM) sector in the UK. * Career Growth: Excellent opportunities for professional development and genuine career progression within a leading and expanding company.
      Job Title: Business Development Manager (Healthcare) My clients seeking a highly motivated and results-driven Business Development Manager to join their team at their head office in Dartford. * Performance Reporting: Prepare and present regular, insightful reports on pipeline health, lead generation efforts, sales performance, and overall business development progress to senior management. * Strategic Development: Design, implement, and execute comprehensive business development plans aimed at achieving and exceeding company revenue targets and growth objectives. * Experience: Minimum of 5 years of proven business development or sales experience, specifically within the hard facilities management (FM) sector in the UK. * Career Growth: Excellent opportunities for professional development and genuine career progression within a leading and expanding company.
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      Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
      Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
      more
      NEW
      The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
      The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. We are seeking several Medical Directors to join our dynamic team. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials including feasibility ...
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      What is the average salary for API in South East?

      Average salary per year
      £67,499

      The average salary for a API in South East is £67,499. API in South East salaries range from £52,499 to £82,499.

      Frequently Asked Questions

      How many contract API jobs are there in South East?
      There are 2 contract API jobs within 30 miles of South East available on EmedCareers right now.

      What other similar jobs are there to contract API jobs in South East?
      As well as contract API jobs in South East, you can find contract Customer Service, Home Management, Management, amongst many others.