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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
3 exact matches jobs are outside your preferred location
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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.
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Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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;
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.
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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
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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.
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We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
We're seeking aProject Managero help us take vision to value and create lasting impact for one of our life sciences managed accounts - As the Project Manager, you will lead the end-to-end delivery of a confidential project scheduled to go live on July 1, 2027. * 10+ years of experience as a Project Manager, with a strong understanding of data and analytics, finance, and legal knowledge - You will develop and manage comprehensive project plans, coordinate internal and external teams, and oversee risk and issue management. Additionally, you will engage stakeholders, ensure quality and governance throughout the project lifecycle, and manage meetings, communications, and documentation across multiple business functions and third-party stakeholders * Develop and manage comprehensive project plans to ensure the successful delivery of the confidential project
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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
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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.
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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
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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
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Leading a team of Data Scientists and AI specialists - You'll lead a growing Data science function responsible for delivering real-world AI, machine learning and data science solutions across a complex professional services environment. * Defining Data & AI strategy and technical direction - To be successful, you'll need a strong background in Data Science, Machine Learning and modern AI technologies, combined with the communication skills to operate confidently from technical workshops through to executive-level discussions. If you can articulate complex AI concepts in 30 seconds, influence stakeholders at every level, and lead a team focused on solving difficult business problems with data - please apply. Most data leadership roles sit at one end of the spectrum. The next phase involves expanding AI capability, shaping a longer-term roadmap around emerging technologies such ...
Leading a team of Data Scientists and AI specialists - You'll lead a growing Data science function responsible for delivering real-world AI, machine learning and data science solutions across a complex professional services environment. * Defining Data & AI strategy and technical direction - To be successful, you'll need a strong background in Data Science, Machine Learning and modern AI technologies, combined with the communication skills to operate confidently from technical workshops through to executive-level discussions. If you can articulate complex AI concepts in 30 seconds, influence stakeholders at every level, and lead a team focused on solving difficult business problems with data - please apply. Most data leadership roles sit at one end of the spectrum. The next phase involves expanding AI capability, shaping a longer-term roadmap around emerging technologies such ...
FEATURED
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;
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project ...
Medpace is currently seeking candidates with 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 ...
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 ...
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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 ...
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
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The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output and/or QC of requested output, is the - The main focus of this role. This individual, working closely with the study statistician, will be responsible for review and acceptance of contract research organization (CRO) deliverables, which are mainly, but not limited to, datasets in submission-ready standard format (ADaM), tables, figures, and listings, and submission packages. This individual will participate in the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for all requested analyses.
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output and/or QC of requested output, is the - The main focus of this role. This individual, working closely with the study statistician, will be responsible for review and acceptance of contract research organization (CRO) deliverables, which are mainly, but not limited to, datasets in submission-ready standard format (ADaM), tables, figures, and listings, and submission packages. This individual will participate in the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for all requested analyses.
Job Summary - Do you have a passion for Artificial Intelligence (AI) and are looking to make a difference in how the latest clinical trials progress into the market? Do you have a background in data science and/or computer science with experience working with AI tools for interactive AI applications across various IT systems? If so, we have an exciting opportunity for you to help take the reins of a groundbreaking project at Medpace. We are currently seeking a professional with direct experience interacting with artificial intelligence (AI) tools such as NLP, LLM, IA etc. This professional will be expected to lead the programming and fine-tuning of various AI tools and help IT teams to implement them into new applications. This professional will work collaboratively across the organization with multiple teams to help design the roadmap for how AI can improve efficiency of company ...
Job Summary - Do you have a passion for Artificial Intelligence (AI) and are looking to make a difference in how the latest clinical trials progress into the market? Do you have a background in data science and/or computer science with experience working with AI tools for interactive AI applications across various IT systems? If so, we have an exciting opportunity for you to help take the reins of a groundbreaking project at Medpace. We are currently seeking a professional with direct experience interacting with artificial intelligence (AI) tools such as NLP, LLM, IA etc. This professional will be expected to lead the programming and fine-tuning of various AI tools and help IT teams to implement them into new applications. This professional will work collaboratively across the organization with multiple teams to help design the roadmap for how AI can improve efficiency of company ...
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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 ...
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A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
A senior leadership opportunity within a global professional services organisation investing heavily in Data & AI. This is a hands-on leadership role combining Data Science, GenAI, Solution Architecture and stakeholder engagement, focused on delivering AI-powered solutions that drive measurable business impact. * Define the technical strategy for Data & AI initiatives across the business * Mentor Data Scientists and provide technical leadership across delivery teams - You'll play a key role in shaping and delivering the firm's AI roadmap, working closely with senior stakeholders to identify high-value use cases and take them from concept through to production. * Translate complex business challenges into scalable AI products and capabilities * Deliver AI use cases across document intelligence, knowledge search, workflow automation and AI assistants
FEATURED