Date posted
Commute time
Locations
Type of Company
Job types
Salaries
Locations
Locations
Salaries
Date posted
Type of Company
Job types
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
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.
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
)
The 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.
)
Technology COO Manager / CTO Office Manager (Contract)
Technology COO Manager / CTO Office Manager (Contract)
Essential Consulting
Sheffield (S1)
From £550 to £600 per day (inside IR35)
Technology COO Manager / CTO Office Manager We are looking to onboard an experienced Technology COO Manager / CTO Office Manager to support a large-scale technology organisation within a leading global financial services environment. * Strong experience within Technology COO, CTO Office, CIO Office, Technology Business Management or Technology Operations functions - Likely to suit candidates currently working within Technology COO, CTO Office, CIO Office or Technology Business Management functions in large banking or financial services organisations. This role combines elements of Technology COO, Business Management, Operations Management and Internal Consulting, making it ideally suited to candidates who enjoy solving problems, driving improvements and operating at the intersection of strategy and execution. * 6 month initial contract with strong potential for extension * Sheffield - hybrid
Technology COO Manager / CTO Office Manager We are looking to onboard an experienced Technology COO Manager / CTO Office Manager to support a large-scale technology organisation within a leading global financial services environment. * Strong experience within Technology COO, CTO Office, CIO Office, Technology Business Management or Technology Operations functions - Likely to suit candidates currently working within Technology COO, CTO Office, CIO Office or Technology Business Management functions in large banking or financial services organisations. This role combines elements of Technology COO, Business Management, Operations Management and Internal Consulting, making it ideally suited to candidates who enjoy solving problems, driving improvements and operating at the intersection of strategy and execution. * 6 month initial contract with strong potential for extension * Sheffield - hybrid
NEW
)
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 ...
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
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
)
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
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 ...
)
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.
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 ...
As a Data Engineer, you will play a crucial role in optimising and enhancing our data pipelines, ensuring efficient data processing, storage and retrieval. We seek a skilled and motivated Data Engineer to join our dynamic team. PDBe is a founding partner of the Worldwide Protein Data Bank organisation, which maintains the global archive of 3D structural data on macromolecules the Protein Data Bank (PDB). The PDBe team is international and inter-disciplinary and consists of expert data curators, bioinformaticians, scientific software developers and IT specialists. You will work closely with cross-functional teams to analyse requirements, propose new data pipeline architectures, and implement solutions to improve performance and scalability. * Analyse existing data pipelines and identify areas for improvement, optimisation, and scalability.
As a Data Engineer, you will play a crucial role in optimising and enhancing our data pipelines, ensuring efficient data processing, storage and retrieval. We seek a skilled and motivated Data Engineer to join our dynamic team. PDBe is a founding partner of the Worldwide Protein Data Bank organisation, which maintains the global archive of 3D structural data on macromolecules the Protein Data Bank (PDB). The PDBe team is international and inter-disciplinary and consists of expert data curators, bioinformaticians, scientific software developers and IT specialists. You will work closely with cross-functional teams to analyse requirements, propose new data pipeline architectures, and implement solutions to improve performance and scalability. * Analyse existing data pipelines and identify areas for improvement, optimisation, and scalability.
PREMIUM
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
)
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
FEATURED
)
We are seeking a Senior Data Scientist with a strong background in Biostatistics to help leading life sciences and pharmaceutical organisations modernise and scale their statistical modelling capabilities. You'll work closely with biostatisticians, data scientists, and technical stakeholders to improve modelling approaches and deploy scalable solutions within cloud-based environments. This role combines statistical expertise with modern data engineering practices, enabling the development of robust, reproducible, and production-ready analytical solutions. * Experience with Databricks or similar cloud data platforms - London, UK (Hybrid 23 days per week) Up to £80,000 + Benefits - The Opportunity - Key Responsibilities * Partner with biostatisticians and cross-functional teams to enhance statistical modelling methodologies * Design and develop scalable R-based modelling workflows and packages
We are seeking a Senior Data Scientist with a strong background in Biostatistics to help leading life sciences and pharmaceutical organisations modernise and scale their statistical modelling capabilities. You'll work closely with biostatisticians, data scientists, and technical stakeholders to improve modelling approaches and deploy scalable solutions within cloud-based environments. This role combines statistical expertise with modern data engineering practices, enabling the development of robust, reproducible, and production-ready analytical solutions. * Experience with Databricks or similar cloud data platforms - London, UK (Hybrid 23 days per week) Up to £80,000 + Benefits - The Opportunity - Key Responsibilities * Partner with biostatisticians and cross-functional teams to enhance statistical modelling methodologies * Design and develop scalable R-based modelling workflows and packages
)
We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
FEATURED
)
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
Medpace is currently seeking candidates with Renal 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 Renal 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 ...
)
Technical Manager
Technical Manager
TREVETT PROFESSIONAL SERVICES LTD
Euston, North West London (NW1), NW1 2BE
£65,000 per annum
Reporting to the Technical Director, the Technical Manager will be responsible for the management and control of all technical matters relating to plant and equipment maintenance including existing equipment, new works and future upgrade works. Trevett Services are delighted to be partnering with a leading Service Provider to source a Technical Manager for central London. Working in an iconic London building, the Technical Manager will lead on the delivery of M&E Maintenance Projects and Building Services Lifecycle Projects. My client is looking for a detail-oriented and well organised Technical Manager with excellent communication and stakeholder management skills as well as having good report writing skills. Central London £65k + benefits - About you:You will be qualified in either Electrical or Mechanical EngineeringExperience of managing multi-disciplined engineering teams
Reporting to the Technical Director, the Technical Manager will be responsible for the management and control of all technical matters relating to plant and equipment maintenance including existing equipment, new works and future upgrade works. Trevett Services are delighted to be partnering with a leading Service Provider to source a Technical Manager for central London. Working in an iconic London building, the Technical Manager will lead on the delivery of M&E Maintenance Projects and Building Services Lifecycle Projects. My client is looking for a detail-oriented and well organised Technical Manager with excellent communication and stakeholder management skills as well as having good report writing skills. Central London £65k + benefits - About you:You will be qualified in either Electrical or Mechanical EngineeringExperience of managing multi-disciplined engineering teams
)
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
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
)
Senior Data Scientist
Senior Data Scientist
MASS Consultants
Little Paxton, St. Neots (PE19)
From £45,000 to £65,000 per annum DOE plus company benefits
As our Data Intelligence capability continues to grow, we're looking for a Senior Data Scientist to join the team and support the delivery of innovative data solutions across a range of exciting customer projects. As a Senior Data Scientist, you'll provide technical leadership across a variety of projects, taking ownership of delivery while helping to guide and develop less experienced team members. Based at our head office in Little Paxton, St Neots, you'll work alongside a highly skilled team of Data Scientists, Software Engineers and Technical Specialists, delivering innovative solutions for highly secure customers. You'll play a key role in delivering advanced data science capabilities, helping customers unlock value from complex datasets through analysis, visualisation, modelling, prediction and AI-driven solutions.
As our Data Intelligence capability continues to grow, we're looking for a Senior Data Scientist to join the team and support the delivery of innovative data solutions across a range of exciting customer projects. As a Senior Data Scientist, you'll provide technical leadership across a variety of projects, taking ownership of delivery while helping to guide and develop less experienced team members. Based at our head office in Little Paxton, St Neots, you'll work alongside a highly skilled team of Data Scientists, Software Engineers and Technical Specialists, delivering innovative solutions for highly secure customers. You'll play a key role in delivering advanced data science capabilities, helping customers unlock value from complex datasets through analysis, visualisation, modelling, prediction and AI-driven solutions.