Date posted
Commute time
Locations
Type of Company
Job types
Salaries
Locations
)
Protein Function Development Team Leader
Protein Function Development Team Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £89,499 to £114,027 per annum
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
NEWPREMIUM
1 exact match is outside your preferred location
)
Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
Broad and expert knowledge of analytical methodologies supporting API development. The site includes state-of-the-art GMP facilities for API development, oral solid dose manufacture, formulation development, and process chemistry.
These jobs might also interest you
)
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 ...
)
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
)
As a Senior Scientist in Protein and Cell Sciences, you will design, express, purify and characterize recombinant proteins that underpin antibody discovery and other biologics programs. Are you ready to turn recombinant protein design into therapies that change the way cancer is treated? You will use modern computational tools alongside rigorous experimental methods to ensure the proteins you produce behave as intended. * Recombinant Antigen Design: Apply computational structural biology (including AlphaFold and ProteinMPNN) to design target proteins that are fit-for-purpose for discovery and development. * Protein Production: Express and purify recombinant proteins using bacterial and transient mammalian systems (E.coli, HEK, CHO), building robust, scalable methods and standard operating procedures that improve throughput and reproducibility.
As a Senior Scientist in Protein and Cell Sciences, you will design, express, purify and characterize recombinant proteins that underpin antibody discovery and other biologics programs. Are you ready to turn recombinant protein design into therapies that change the way cancer is treated? You will use modern computational tools alongside rigorous experimental methods to ensure the proteins you produce behave as intended. * Recombinant Antigen Design: Apply computational structural biology (including AlphaFold and ProteinMPNN) to design target proteins that are fit-for-purpose for discovery and development. * Protein Production: Express and purify recombinant proteins using bacterial and transient mammalian systems (E.coli, HEK, CHO), building robust, scalable methods and standard operating procedures that improve throughput and reproducibility.
NEW
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 ...
HR Systems Solution Expert (Workday HCM)
HR Systems Solution Expert (Workday HCM)
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £48,703 to £68,017 per annum
Following the successful launch of our Workday HR Core platform, we're continuing our organisation-wide Workday journey and are looking for an experienced HR Systems Solution Expert to help shape the future of our people processes. As our HR Systems Solution Expert, you'll act as the vital link between HR business needs and technical system delivery. * Troubleshoot complex HR systems issues and provide expert guidance on best practice. This is an exciting opportunity for an HR professional who combines strong operational HR knowledge with a passion for systems, process improvement and technology. Working at the intersection of HR and digital transformation, you'll help design and optimise HR solutions that support a world-leading international research organisation. * Partner with HR, ERP and IT colleagues to gather and translate business requirements into Workday solutions.
Following the successful launch of our Workday HR Core platform, we're continuing our organisation-wide Workday journey and are looking for an experienced HR Systems Solution Expert to help shape the future of our people processes. As our HR Systems Solution Expert, you'll act as the vital link between HR business needs and technical system delivery. * Troubleshoot complex HR systems issues and provide expert guidance on best practice. This is an exciting opportunity for an HR professional who combines strong operational HR knowledge with a passion for systems, process improvement and technology. Working at the intersection of HR and digital transformation, you'll help design and optimise HR solutions that support a world-leading international research organisation. * Partner with HR, ERP and IT colleagues to gather and translate business requirements into Workday solutions.
NEWPREMIUM
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - 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. * Psychiatry
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - 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. * Psychiatry
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 ...
)
Our client is looking for a Senior Development Scientist who has navigated the full journey from early-stage concept to commercially viable product - and wants to do it again, at pace, in a high-growth environment. You'll be a key member of the development team, responsible for shaping technical direction and driving delivery across the full product development lifecycle. * Provide day-to-day technical leadership and line management, developing the scientists around you * A clear track record of taking biological products or workflows from early development through to robust, commercially deployed solutions * Proven ability to lead, mentor, and manage scientists in a fast-moving commercial or industrial setting * Excellent communication skills, with the credibility to engage senior leadership and the clarity to support junior team members
Our client is looking for a Senior Development Scientist who has navigated the full journey from early-stage concept to commercially viable product - and wants to do it again, at pace, in a high-growth environment. You'll be a key member of the development team, responsible for shaping technical direction and driving delivery across the full product development lifecycle. * Provide day-to-day technical leadership and line management, developing the scientists around you * A clear track record of taking biological products or workflows from early development through to robust, commercially deployed solutions * Proven ability to lead, mentor, and manage scientists in a fast-moving commercial or industrial setting * Excellent communication skills, with the credibility to engage senior leadership and the clarity to support junior team members
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
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 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 ...
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 London, 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 London, 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 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
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
)
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.
InterPro/Pfam Software Project Leader
InterPro/Pfam Software Project Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £57,520 to £77,212 per annum
We are seeking to hire an InterPro/Pfam Software Project leader to lead a cultural and technical shift towards AI-first development, leveraging AI coding assistants and generative tools to accelerate delivery, improve code quality, and reduce technical debt across both platforms. In your role, you will lead the software development team responsible for the Pfam and InterPro databases. Reporting to the Head of the Protein Families Group at EMBL-EBI, this role sits at the intersection of cutting-edge bioinformatics and modern software engineering. The team currently comprises of several software developers and engineers. * Lead the Pfam/InterPro software development team, managing workload, priorities, and professional development. * Drive the transition to AI-first software development practices, embedding AI coding tools (e.g. Claude Code, GitHub Copilot) into production workflows.
We are seeking to hire an InterPro/Pfam Software Project leader to lead a cultural and technical shift towards AI-first development, leveraging AI coding assistants and generative tools to accelerate delivery, improve code quality, and reduce technical debt across both platforms. In your role, you will lead the software development team responsible for the Pfam and InterPro databases. Reporting to the Head of the Protein Families Group at EMBL-EBI, this role sits at the intersection of cutting-edge bioinformatics and modern software engineering. The team currently comprises of several software developers and engineers. * Lead the Pfam/InterPro software development team, managing workload, priorities, and professional development. * Drive the transition to AI-first software development practices, embedding AI coding tools (e.g. Claude Code, GitHub Copilot) into production workflows.
PREMIUM
)
As a Principal Researcher, you are expected to shape the strategic vision of our research initiatives and drive transformative breakthroughs in AI. Principal Researchers are leaders who mentor senior staff, set policy, and ensure our research has a lasting impact on both the company and the broader scientific community. * Mentor and provide leadership to senior researchers and research teams - This role is suited for individuals who excel at influencing organizational research priorities, overseeing multiple projects, and representing the team in high-level external partnerships. * Applying AI to the design and optimization of semiconductors * Conducting fundamental research that supports both our applications and the broader scientific community Current areas of interest include large language models (LLMs), optimization methods for deep learning, reinforcement learning (RL), and ...
As a Principal Researcher, you are expected to shape the strategic vision of our research initiatives and drive transformative breakthroughs in AI. Principal Researchers are leaders who mentor senior staff, set policy, and ensure our research has a lasting impact on both the company and the broader scientific community. * Mentor and provide leadership to senior researchers and research teams - This role is suited for individuals who excel at influencing organizational research priorities, overseeing multiple projects, and representing the team in high-level external partnerships. * Applying AI to the design and optimization of semiconductors * Conducting fundamental research that supports both our applications and the broader scientific community Current areas of interest include large language models (LLMs), optimization methods for deep learning, reinforcement learning (RL), and ...
)
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
)
Project Manager / Benefits Manager – IS8 Life Science Programme
Project Manager / Benefits Manager – IS8 Life Science Programme
UKRI
Swindon, Wiltshire
£37841 Per annum
As the Life Sciences Project Manager / Benefits Manager, you will work with colleagues across UKRI to help deliver strategic government and societal priorities through the UKRI Life Sciences programme. To support the effective management, delivery, and coordination of the UKRI Life Sciences Industrial Strategy programme. You will play a key role in programme and project governance, ensuring that intended benefits and outcomes are successfully achieved. * Coordinating and delivering the relevant programmes various projects, dependencies (internal and external), key milestones, risks, governance, financial management, and benefits planning * Developing project specific benefits realisation plans to ensure realisation of benefits for programmes through planning and designing and ensuring that project outputs meet programme requirements.
As the Life Sciences Project Manager / Benefits Manager, you will work with colleagues across UKRI to help deliver strategic government and societal priorities through the UKRI Life Sciences programme. To support the effective management, delivery, and coordination of the UKRI Life Sciences Industrial Strategy programme. You will play a key role in programme and project governance, ensuring that intended benefits and outcomes are successfully achieved. * Coordinating and delivering the relevant programmes various projects, dependencies (internal and external), key milestones, risks, governance, financial management, and benefits planning * Developing project specific benefits realisation plans to ensure realisation of benefits for programmes through planning and designing and ensuring that project outputs meet programme requirements.
NEW
)
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
)
We are seeking experienced electronics Lab Manager to lead, operate, and continuously evolve our electronics and hardware engineering lab. You will act as the owner of the lab environmentresponsible for its infrastructure, safety, equipment budgets and lifecycle, documentation, and operational strategy. This role is deeply hands-on and requires strong technical expertise and the ability to build long-term foundations for a high-performance lab. Lab Ownership & Operations * Own the end-to-end operation of the electronics/hardware lab, ensuring high availability, reliability, and readiness. * Oversee lab infrastructure: server racks, boards, test equipment, instruments, power distribution, network integration, thermal/airflow constraints, and monitoring systems. * Define, document, and maintain lab Standard Operating Procedures (SOPs), workflows, and access policies.
We are seeking experienced electronics Lab Manager to lead, operate, and continuously evolve our electronics and hardware engineering lab. You will act as the owner of the lab environmentresponsible for its infrastructure, safety, equipment budgets and lifecycle, documentation, and operational strategy. This role is deeply hands-on and requires strong technical expertise and the ability to build long-term foundations for a high-performance lab. Lab Ownership & Operations * Own the end-to-end operation of the electronics/hardware lab, ensuring high availability, reliability, and readiness. * Oversee lab infrastructure: server racks, boards, test equipment, instruments, power distribution, network integration, thermal/airflow constraints, and monitoring systems. * Define, document, and maintain lab Standard Operating Procedures (SOPs), workflows, and access policies.
NEW
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;