Date posted
Commute time
Locations
Type of Company
Job types
Salaries
Locations
Filters
Sort byRelevance
Locations
Salaries
Date posted
Type of Company
Job types
Locations
There is no job matching your search
Api
Ipswich
No need to fret! We’re adding new jobs every single day. Find out immediately when we’ve found a match for you.
1 exact match is outside your preferred location
)
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 ...
PREMIUM
These jobs might also interest you
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
)
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.
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.
PREMIUM
We are looking for a Research Pipeline Project Manager to join our team. In GSK, the Pipeline Project Manager (PPM) will partner with project leads to help teams plot the best course, then accelerate through complexity and uncertainty with no compromise to quality or safety. You will lead and coordinate cross-functional research pre-clinical pipeline projects that advance our scientific priorities. * Lead end-to-end planning and delivery for assigned research pipeline projects, with clear owners, milestones and measurable outcomes. * Support handover of projects from research into later development or operational teams, ensuring knowledge transfer and acceptance criteria are met. Pipeline Project Management drives decisions and enables teams to choose the best path and deliver medicines to patients faster than ever.
We are looking for a Research Pipeline Project Manager to join our team. In GSK, the Pipeline Project Manager (PPM) will partner with project leads to help teams plot the best course, then accelerate through complexity and uncertainty with no compromise to quality or safety. You will lead and coordinate cross-functional research pre-clinical pipeline projects that advance our scientific priorities. * Lead end-to-end planning and delivery for assigned research pipeline projects, with clear owners, milestones and measurable outcomes. * Support handover of projects from research into later development or operational teams, ensuring knowledge transfer and acceptance criteria are met. Pipeline Project Management drives decisions and enables teams to choose the best path and deliver medicines to patients faster than ever.
)
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 ...
)
Senior Principal Scientist / Director – Computational Chemistry (IDD)
Senior Principal Scientist / Director – Computational Chemistry (IDD)
Pharmaron
Hoddesdon, Hertfordshire
Competitive
Pharmaron is looking for a Senior Principal Scientist / Director Computational Chemistry to lead on the design and optimisation of multi-modality ligands within our Integrated Drug Discovery programmes and help shape our Computational Sciences capability. * Deep knowledge of computational chemistry in drug discovery * Strong understanding of medicinal chemistry, biology and DMPK integration - This is a senior role requiring scientific excellence, and client engagement to drive integrated, multi-modality drug discovery programmes. The team comprises scientific expertise and strategic leadership across medicinal chemistry, CADD, biology, DMPK and translational science. Working closely with our partners, we define strategy, coordinate execution across teams and, with an AI enabled accelerated DesignMakeTestAnalyse cycle, support the progression of projects and innovative ...
Pharmaron is looking for a Senior Principal Scientist / Director Computational Chemistry to lead on the design and optimisation of multi-modality ligands within our Integrated Drug Discovery programmes and help shape our Computational Sciences capability. * Deep knowledge of computational chemistry in drug discovery * Strong understanding of medicinal chemistry, biology and DMPK integration - This is a senior role requiring scientific excellence, and client engagement to drive integrated, multi-modality drug discovery programmes. The team comprises scientific expertise and strategic leadership across medicinal chemistry, CADD, biology, DMPK and translational science. Working closely with our partners, we define strategy, coordinate execution across teams and, with an AI enabled accelerated DesignMakeTestAnalyse cycle, support the progression of projects and innovative ...
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
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 ...
)
Manager, Translational Biomarker Data Pathways and Re-use
Manager, Translational Biomarker Data Pathways and Re-use
GlaxoSmithKline
Stevenage, Hertfordshire
Competitive
A key objective of this role is to help evolve translational biomarker datasets from one-off outputs into reusable, accessible data assets; available, interpretable and usable across multiple translational use cases. * Translational dataset use & re-use at scale (core accountability): Lead the end-to-end enablement of biomarker dataset re-use (clinical & non-clinical)by helping ensure data is findable, accessible, interpretable and aligned to translational decision-making timelines. * E2E data pathway delivery: When needed, lead the set-up and delivery of complex end-to-end biomarker data pathways across multiple functions, defining data flows, roles, responsibilities and dependencies. * Significant experience working with human biomarker or high-dimensional data types in Pharma/Biotech, academia, healthcare, or a similar complex R&D environment.
A key objective of this role is to help evolve translational biomarker datasets from one-off outputs into reusable, accessible data assets; available, interpretable and usable across multiple translational use cases. * Translational dataset use & re-use at scale (core accountability): Lead the end-to-end enablement of biomarker dataset re-use (clinical & non-clinical)by helping ensure data is findable, accessible, interpretable and aligned to translational decision-making timelines. * E2E data pathway delivery: When needed, lead the set-up and delivery of complex end-to-end biomarker data pathways across multiple functions, defining data flows, roles, responsibilities and dependencies. * Significant experience working with human biomarker or high-dimensional data types in Pharma/Biotech, academia, healthcare, or a similar complex R&D environment.
Medpace is currently seeking candidates with Gastrointestinal related 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 ...
Medpace is currently seeking candidates with Gastrointestinal related 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 ...
)
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.
We are seeking an Pulmonologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. **All Medical Directors have hybrid work from home flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials ...
We are seeking an Pulmonologist - Medical Director to join our dynamic team. The Medical Director will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Medical Director will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. **All Medical Directors have hybrid work from home flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts; * Coordinate with other departments in all phases of the studies and trials ...
)
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 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 ...
)
Johnson & Johnson is currently seeking a Senior Scientist Clinical Pharmacokinetics (PK Scientist) to join our team. The Senior Scientist Clinical Pharmacokinetics (PK Scientist) role within Clinical Pharmacology and Pharmacometrics (CPP) is responsible for (in collaboration with the CPP Leader), the following activities of end-to-end Phase 1 study execution of Clinical Pharmacology Phase 1-owned studies including: protocol development, pharmacokinetic/pharmacodynamic data analysis, and generating the in-text tables and figures and PK/PD attachments for clinical study reports and CP CSR section writing, as well as study summary contributions to CTD regulatory submission documents. The PK Scientist role is also responsible for PK/PD NCA for all study phases (Phase I-IV). * Provide QC review of protocols written by other CPP PK Scientists.
Johnson & Johnson is currently seeking a Senior Scientist Clinical Pharmacokinetics (PK Scientist) to join our team. The Senior Scientist Clinical Pharmacokinetics (PK Scientist) role within Clinical Pharmacology and Pharmacometrics (CPP) is responsible for (in collaboration with the CPP Leader), the following activities of end-to-end Phase 1 study execution of Clinical Pharmacology Phase 1-owned studies including: protocol development, pharmacokinetic/pharmacodynamic data analysis, and generating the in-text tables and figures and PK/PD attachments for clinical study reports and CP CSR section writing, as well as study summary contributions to CTD regulatory submission documents. The PK Scientist role is also responsible for PK/PD NCA for all study phases (Phase I-IV). * Provide QC review of protocols written by other CPP PK Scientists.
NEW
)
As a Senior Scientist I or II within our In-Vitro Biology team based in Portishead, youll be working independently under strategic guidance with understanding and application of scientific and technical standards, principles, theories, concepts, and techniques in a predominantly lab-based environment. Are you a scientist passionate about working with primary human immune cells? Able to communicate effectively across peers, embodying the Charles River Values daily, and acting as a role model in their position and to Technicians, Associate Scientists, Scientists I and II. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND.
As a Senior Scientist I or II within our In-Vitro Biology team based in Portishead, youll be working independently under strategic guidance with understanding and application of scientific and technical standards, principles, theories, concepts, and techniques in a predominantly lab-based environment. Are you a scientist passionate about working with primary human immune cells? Able to communicate effectively across peers, embodying the Charles River Values daily, and acting as a role model in their position and to Technicians, Associate Scientists, Scientists I and II. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND.
NEW
Computational Biologist / Bioinformatician - Chemical Biology Services
Computational Biologist / Bioinformatician - Chemical Biology Services
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £43,015 to £68,017 per annum Salary dependent on experience
We are looking for a highly motivated Computational Biologist / Bioinformatician to join the Chemical Biology Resources team at the European Bioinformatics Institute (EMBL-EBI), located on the Wellcome Genome Campus near Cambridge, as part of the Wellcome Trust funded LIGMAP project, a multi-disciplinary collaboration between University College London and EMBL-EBI. EMBL-EBI provides freely available data from life science experiments, performs basic research in computational biology and offers an extensive user training programme, supporting researchers in academic and industry. The Chemical Biology Resources team provides world-leading chemogenomics resources to the scientific community. ChEMBL is a database of quantitative small-molecule bioactivity data curated primarily from the scientific literature widely used to support drug discovery projects in industry and academia.
We are looking for a highly motivated Computational Biologist / Bioinformatician to join the Chemical Biology Resources team at the European Bioinformatics Institute (EMBL-EBI), located on the Wellcome Genome Campus near Cambridge, as part of the Wellcome Trust funded LIGMAP project, a multi-disciplinary collaboration between University College London and EMBL-EBI. EMBL-EBI provides freely available data from life science experiments, performs basic research in computational biology and offers an extensive user training programme, supporting researchers in academic and industry. The Chemical Biology Resources team provides world-leading chemogenomics resources to the scientific community. ChEMBL is a database of quantitative small-molecule bioactivity data curated primarily from the scientific literature widely used to support drug discovery projects in industry and academia.
PREMIUM
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 Senior Scientist is responsible for leading and directing new product development projects as well as bringing scientific experiste to support our customers for our expanding magnetic beads portfolio. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danahers 15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact. Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental ...
The Senior Scientist is responsible for leading and directing new product development projects as well as bringing scientific experiste to support our customers for our expanding magnetic beads portfolio. Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danahers 15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact. Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental ...
NEW
)
Senior Data Scientist
Senior Data Scientist
Kennedy Pearce Consulting
South West London (SW1V), SW1V
£600 - £700 per day OUTSIDE IR35
They are looking for 2 x Data Scientists to join a high-impact project focused on developing next-generation AI products across multiple global brands. The business offers the scale, backing, and data availability of a global organisation, while giving engineers and data scientists strong ownership over product direction and delivery. You'll join a team of 3 focused specifically on the project, sitting within a wider 25-person Data & AI function. We're partnered with one of the world's largest information, publishing, events, and market intelligence businesses, who are building out a brand new AI project team within one of their core business units. This role sits outside IR35. The Project * Chatbot and conversational AI development * Agentic AI systems * LLM-driven product development * AI-powered B2B marketing agents * Multi-brand AI integrations and workflows
They are looking for 2 x Data Scientists to join a high-impact project focused on developing next-generation AI products across multiple global brands. The business offers the scale, backing, and data availability of a global organisation, while giving engineers and data scientists strong ownership over product direction and delivery. You'll join a team of 3 focused specifically on the project, sitting within a wider 25-person Data & AI function. We're partnered with one of the world's largest information, publishing, events, and market intelligence businesses, who are building out a brand new AI project team within one of their core business units. This role sits outside IR35. The Project * Chatbot and conversational AI development * Agentic AI systems * LLM-driven product development * AI-powered B2B marketing agents * Multi-brand AI integrations and workflows
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 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
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 ...
)
Contract Microsoft Copilot & AI Adoption Consultant We are seeking experienced Microsoft Copilot and AI Adoption Consultants to support a growing portfolio of healthcare and public sector transformation programmes. Successful candidates will help organisations prepare for, deploy and maximise the value of Microsoft Copilot and emerging AI technologies. This is an excellent opportunity to join a growing AI consulting capability and help organisations realise the benefits of Microsoft Copilot and emerging AI technologies. - Deliver Microsoft Copilot readiness assessments. - Experience delivering Microsoft 365 and/or Copilot programmes. - Support AI governance and adoption activities. - Management Consultant - M365 Consultant - Digital Transformation Consultant Location: UK Wide / Hybrid - Contract Type: Contract - Sector: Healthcare & Public Sector - Overview - Key Responsibilities
Contract Microsoft Copilot & AI Adoption Consultant We are seeking experienced Microsoft Copilot and AI Adoption Consultants to support a growing portfolio of healthcare and public sector transformation programmes. Successful candidates will help organisations prepare for, deploy and maximise the value of Microsoft Copilot and emerging AI technologies. This is an excellent opportunity to join a growing AI consulting capability and help organisations realise the benefits of Microsoft Copilot and emerging AI technologies. - Deliver Microsoft Copilot readiness assessments. - Experience delivering Microsoft 365 and/or Copilot programmes. - Support AI governance and adoption activities. - Management Consultant - M365 Consultant - Digital Transformation Consultant Location: UK Wide / Hybrid - Contract Type: Contract - Sector: Healthcare & Public Sector - Overview - Key Responsibilities
NEWPREMIUM