Date posted
Commute time
Locations
Type of Company
Job types
Salaries
Locations
Locations
Salaries
Date posted
Type of Company
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.
3 exact matches jobs are 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.
Google Measurement Protocol & other server-side API technologies.
Google Measurement Protocol & other server-side API technologies.
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
)
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.
)
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
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 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 ...
)
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
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.
NEW
)
Strategy & CDD Industrial Products, Technology & Services - Manager / Consultant
Strategy & CDD Industrial Products, Technology & Services - Manager / Consultant
BDO
City of London (EC1)
competitive salary and package
You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
You will join our Industrial Products, Technology & Services team as a Manager, playing a key role across Project Delivery, Business Development, Thought Leadership, and Practice Development within the Strategy & Commercial Due Diligence (CDD) practice. As a Manager in our growing Industrial Products, Technology & Services team, you will play a key role in Project Delivery, Business Development, Thought Leadership and Practice Development, working with a dedicated team of sector-focused professionals. * B2B / industrials / manufacturing Sector experience - in particular deals and growth strategy experience - Our Advisory team provide a wide variety of services that deliver value-led advice and outcomes. The team work across strategy, operations and improvement as well as at a transactional and defined project level. From technology to risk advisory, they’re experts in following through on ...
NEWPREMIUM
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
We are seeking an Pulmonologist - 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. **All Medical Directors have hybrid work from home 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 ...
We are seeking an Pulmonologist - 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. **All Medical Directors have hybrid work from home 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 ...
)
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Biostatistics and Statistical Programming Operations - The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions * Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews.
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Biostatistics and Statistical Programming Operations - The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions * Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews.
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.
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;
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 ...
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 ...
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;
)
Director of Governance, Risk and Assurance
Director of Governance, Risk and Assurance
Victim Support
The City, City of London (EC2), EC2A 4BQ
Up to £83000.00 per annum
The Director of Governance, Risk and Assurance is a member of the Senior Leadership Team, holding strategic accountability for governance, risk, assurance and quality across the organisation. This newly established role offers a unique opportunity to shape and strengthen organisational governance, risk and assurance frameworks across a national charity delivering vital services to victims of crime. As Director, you will provide strategic leadership across governance, risk management, compliance and quality assurance, ensuring that the organisation operates safely, effectively and in line with its statutory and regulatory responsibilities. This is an exciting new role that will provide leadership as Victim Support grows, ensuring excellent governance, risk management and assurance across the organisation. If you are passionate about good governance and are looking to lead ...
The Director of Governance, Risk and Assurance is a member of the Senior Leadership Team, holding strategic accountability for governance, risk, assurance and quality across the organisation. This newly established role offers a unique opportunity to shape and strengthen organisational governance, risk and assurance frameworks across a national charity delivering vital services to victims of crime. As Director, you will provide strategic leadership across governance, risk management, compliance and quality assurance, ensuring that the organisation operates safely, effectively and in line with its statutory and regulatory responsibilities. This is an exciting new role that will provide leadership as Victim Support grows, ensuring excellent governance, risk management and assurance across the organisation. If you are passionate about good governance and are looking to lead ...
NEWPREMIUM
)
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.
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in Stirling, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. 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
Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in Stirling, UK. * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables * Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred; We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. 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
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.
Medpace is currently seeking candidates with Oncology 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 ...
Medpace is currently seeking candidates with Oncology 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 ...