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Be the First to Apply - Division - Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. Job Title - Job Description
Be the First to Apply - Division - Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. Job Title - Job Description
Be the First to Apply - Division - Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. Job Title - Job Description
Be the First to Apply - Division - Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. Job Title - Job Description
Productionise models into a reproducible, API-first toolkit; partner with Infrastructure on GPU training and HPC; maintain high standards of ML best practices, including rigorous evaluation, benchmarks, and reproducibility.
Productionise models into a reproducible, API-first toolkit; partner with Infrastructure on GPU training and HPC; maintain high standards of ML best practices, including rigorous evaluation, benchmarks, and reproducibility.
1 exact match is outside your preferred location
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Location: United Kingdom (Remote) Type: 12 months Contract - Rate/Salary: 500 per day - IR35 Status: Outside IR35 - Role Summary - Join a major UK public sector organisation to help expand data science and analytics capability across a high-impact portfolio of services. Deliver advanced analytical models and practical AI/ML solutions that support better decision-making and improved outcomes for the public. Work end-to-end across discovery, data acquisition, modelling, deployment, reporting and continuous improvement. Operate within a controlled and governed environment, producing clear, audit-friendly artefacts and defensible analytical outputs. Remote-first engagement with occasional site visits (as required for workshops, stakeholder sessions, or delivery milestones). What Youll Be Doing - Lead the design and build of data science solutions from problem definition to production-ready ...
Location: United Kingdom (Remote) Type: 12 months Contract - Rate/Salary: 500 per day - IR35 Status: Outside IR35 - Role Summary - Join a major UK public sector organisation to help expand data science and analytics capability across a high-impact portfolio of services. Deliver advanced analytical models and practical AI/ML solutions that support better decision-making and improved outcomes for the public. Work end-to-end across discovery, data acquisition, modelling, deployment, reporting and continuous improvement. Operate within a controlled and governed environment, producing clear, audit-friendly artefacts and defensible analytical outputs. Remote-first engagement with occasional site visits (as required for workshops, stakeholder sessions, or delivery milestones). What Youll Be Doing - Lead the design and build of data science solutions from problem definition to production-ready ...
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Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Scotland, Stirling 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
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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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Senior Laboratory Technician
Senior Laboratory Technician
BAM UK & Ireland
Kilsyth, Glasgow (G65), G65 9BL
Competitive salary & benefits package including company car/allowance.
We are currently looking to recruit Senior Laboratory Technicians at laboratories and projects throughout the UK. * HS2 South Laboratory, Aylesbury, Oxfordshire * HS2 North Laboratory, Greatworth, Northamptonshire * Kilsyth Laboratory, Scotland * Inverness Laboratory, Scotland * Assist with day to day running of mobile site testing/laboratory testing including organising workload, on site sampling and testing. Liaising with laboratory manager to ensure the provision of testing capabilities. * Deliver training/proficiency checks to/for laboratory personnel * Ensure that site sampling and laboratory testing is carried out to high standards of safety, quality and efficiency * Ensure that adequate and proper records are kept and filed correctly to satisfy the requirements of the laboratory management system and UKAS requirements
We are currently looking to recruit Senior Laboratory Technicians at laboratories and projects throughout the UK. * HS2 South Laboratory, Aylesbury, Oxfordshire * HS2 North Laboratory, Greatworth, Northamptonshire * Kilsyth Laboratory, Scotland * Inverness Laboratory, Scotland * Assist with day to day running of mobile site testing/laboratory testing including organising workload, on site sampling and testing. Liaising with laboratory manager to ensure the provision of testing capabilities. * Deliver training/proficiency checks to/for laboratory personnel * Ensure that site sampling and laboratory testing is carried out to high standards of safety, quality and efficiency * Ensure that adequate and proper records are kept and filed correctly to satisfy the requirements of the laboratory management system and UKAS requirements
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The Chemistry Department at Charles River Edinburgh is seeking a talented and flexible individual for a role as a Scientific Associate. The successful applicant will have excellent communication skills, working effectively with others to overcome scientific challenges and learn new skills. For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Job Overview - In order to support our Agrochemical, Animal Health and Pharmaceutical Sponsors, the Chemistry department provides ...
The Chemistry Department at Charles River Edinburgh is seeking a talented and flexible individual for a role as a Scientific Associate. The successful applicant will have excellent communication skills, working effectively with others to overcome scientific challenges and learn new skills. For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, well help you build a career that you can feel passionate about. Job Overview - In order to support our Agrochemical, Animal Health and Pharmaceutical Sponsors, the Chemistry department provides ...
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Medpace is currently seeking candidates with Oncology related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Scotland, Stirling 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 Oncology related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Scotland, Stirling 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 ...
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Associate Clinical Trial Manager (PhD) - Radiopharmaceuticals
Associate Clinical Trial Manager (PhD) - Radiopharmaceuticals
Medpace
Stirling, Stirlingshire
Competitive
Medpace is currently seeking candidates with Radiopharmaceutical or Nuclear Medicine 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
Medpace is currently seeking candidates with Radiopharmaceutical or Nuclear Medicine 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
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you. Responsibilities * Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies;
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you. Responsibilities * Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies;
Senior Laboratory Technician
Senior Laboratory Technician
BAM UK & Ireland
Kilmorack, Beauly (IV4), IV4 7BG
Competitive salary & benefits package including company car/allowance.
We are currently looking to recruit Senior Laboratory Technicians at laboratories and projects throughout the UK. * HS2 South Laboratory, Aylesbury, Oxfordshire * HS2 North Laboratory, Greatworth, Northamptonshire * Kilsyth Laboratory, Scotland * Inverness Laboratory, Scotland * Assist with day to day running of mobile site testing/laboratory testing including organising workload, on site sampling and testing. Liaising with laboratory manager to ensure the provision of testing capabilities. * Deliver training/proficiency checks to/for laboratory personnel * Ensure that site sampling and laboratory testing is carried out to high standards of safety, quality and efficiency * Ensure that adequate and proper records are kept and filed correctly to satisfy the requirements of the laboratory management system and UKAS requirements
We are currently looking to recruit Senior Laboratory Technicians at laboratories and projects throughout the UK. * HS2 South Laboratory, Aylesbury, Oxfordshire * HS2 North Laboratory, Greatworth, Northamptonshire * Kilsyth Laboratory, Scotland * Inverness Laboratory, Scotland * Assist with day to day running of mobile site testing/laboratory testing including organising workload, on site sampling and testing. Liaising with laboratory manager to ensure the provision of testing capabilities. * Deliver training/proficiency checks to/for laboratory personnel * Ensure that site sampling and laboratory testing is carried out to high standards of safety, quality and efficiency * Ensure that adequate and proper records are kept and filed correctly to satisfy the requirements of the laboratory management system and UKAS requirements
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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 ...
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Sitting within the site leadership team, the Laboratory Manager oversees all laboratory operations within a food-grade plastic recycling facility. Job Description: Laboratory Manager The Laboratory Manager plays a key role in supporting sustainable manufacturing processes while maintaining compliance with industry and regulatory standards. Department: Quality / Laboratory Operations - The manager leads a team of lab technicians, manages testing protocols, maintains compliance with relevant standards (e.g., FDA, EFSA,) and supports continuous improvement within the facility. Laboratory Operations & Testing - Develop, implement, and maintain laboratory testing methods, SOPs, and work instructions related to food-grade plastic recycling. Support risk assessments, corrective actions, and preventive measures related to laboratory and production processes.
Sitting within the site leadership team, the Laboratory Manager oversees all laboratory operations within a food-grade plastic recycling facility. Job Description: Laboratory Manager The Laboratory Manager plays a key role in supporting sustainable manufacturing processes while maintaining compliance with industry and regulatory standards. Department: Quality / Laboratory Operations - The manager leads a team of lab technicians, manages testing protocols, maintains compliance with relevant standards (e.g., FDA, EFSA,) and supports continuous improvement within the facility. Laboratory Operations & Testing - Develop, implement, and maintain laboratory testing methods, SOPs, and work instructions related to food-grade plastic recycling. Support risk assessments, corrective actions, and preventive measures related to laboratory and production processes.
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This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
This senior position has a three-year term with a leading research institution and has strong Data Science elements. As a PhD-qualified scientist with further research or commercial experience, you will bring your prior experience in signal processing to bear. * Additional experience in research or commercial R&D (including a leading/mentoring role in some capacity, either for a small team, research project, or supervising PhDs, etc.) The role comes with opportunities for collaborative research into a range of new areas, learning and applying new techniques whilst building your reputation through contributions and publications. R&D applying AI and algorithms to real-world signals/comms, sensor fusion - London, hybrid working; to £58k plus benefits - You'll be helping to establish and further the state of the art, with a view to paving the way for future technology adoption and new applications.
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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
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our UK team and to be based at our growing UK office in Stirling. * Manage Clinical Safety activities and multiple large programs * Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality; * Provide safety review of clinical study documents, including protocols, study reports; and marketing application components. * Bachelors degree or equivalent and clinical safety experience, including project management and ideally line management experience; * Previous experience of managing clinical safety activities for multiple programmes; * Comprehensive knowledge of global clinical safety regulatory requirements; This position plays a key role in the pharmacovigilance process at Medpace.
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our UK team and to be based at our growing UK office in Stirling. * Manage Clinical Safety activities and multiple large programs * Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality; * Provide safety review of clinical study documents, including protocols, study reports; and marketing application components. * Bachelors degree or equivalent and clinical safety experience, including project management and ideally line management experience; * Previous experience of managing clinical safety activities for multiple programmes; * Comprehensive knowledge of global clinical safety regulatory requirements; This position plays a key role in the pharmacovigilance process at Medpace.
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you. Responsibilities * Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies;
Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London or Stirling. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you. Responsibilities * Contribute to clinical development of plan preparation; * Review of study protocol and preparation of statistical methodologies;
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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.
Operate in collaboration with Project Statistician and other Statistical Analysts and Programmers to ensure study outputs are produced to a high quality and in a timely fashion; Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Analyst to join our Global Statistics team. At Medpace, Statistical Analysts go through an extensive onboarding and training process, which prepares them to become experts in their field. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities * Support analysis for global studies; * Review analysis plans for appropriate methods;
Operate in collaboration with Project Statistician and other Statistical Analysts and Programmers to ensure study outputs are produced to a high quality and in a timely fashion; Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Statistical Analyst to join our Global Statistics team. At Medpace, Statistical Analysts go through an extensive onboarding and training process, which prepares them to become experts in their field. Job Summary - This position will work in a team to accomplish tasks and projects that are instrumental to the companys success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities * Support analysis for global studies; * Review analysis plans for appropriate methods;
Clinical Safety Coordinator - Pharmacovigilance / Drug Safety
Clinical Safety Coordinator - Pharmacovigilance / Drug Safety
Medpace
Stirling, Stirlingshire
Competitive
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in Stirling. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
Train new Clinical Safety Coordinators on safety reporting responsibilities - As such, we are searching for motivated individuals to join our Clinical Safety team in Stirling. * SAE reconciliation between safety database and clinical database * Preparation of clinical safety documents as required (i.e., safety management plan, periodic safety reports and presentations) * Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor * Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines - Working as part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines.
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A growing organisation is looking for a Senior Data Scientist to help develop advanced AI and analytics capabilities that power large-scale intelligence and data-driven products. Senior Data Scientist Location: UK Remote - As a Senior Data Scientist, you will contribute to the development and optimisation of advanced machine learning and AI models while maintaining high standards of experimentation, validation, and responsible AI practices. * Apply generative AI and NLP techniques to improve modelling and data extraction capabilities * Perform large-scale data analysis and transformation using SQL and cloud-native technologies * Translate business and product challenges into scalable, data-driven solutions * Strong commercial experience in Data Science, Machine Learning, or Advanced Analytics - Salary: £60,000 - £70,000 - Employment Type: Full-Time - Please note: Sponsorship is not available for this position.
A growing organisation is looking for a Senior Data Scientist to help develop advanced AI and analytics capabilities that power large-scale intelligence and data-driven products. Senior Data Scientist Location: UK Remote - As a Senior Data Scientist, you will contribute to the development and optimisation of advanced machine learning and AI models while maintaining high standards of experimentation, validation, and responsible AI practices. * Apply generative AI and NLP techniques to improve modelling and data extraction capabilities * Perform large-scale data analysis and transformation using SQL and cloud-native technologies * Translate business and product challenges into scalable, data-driven solutions * Strong commercial experience in Data Science, Machine Learning, or Advanced Analytics - Salary: £60,000 - £70,000 - Employment Type: Full-Time - Please note: Sponsorship is not available for this position.
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 a Psychiatry Medical Director 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. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
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 a Psychiatry Medical Director 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. We are currently seeking Medical Directors in different locations. **All Medical Directors have hybrid WFH flexibility. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. * Provide medical management and expertise for clinical trials; * Contribute medical expertise to study reports, regulatory documents, and manuscripts;
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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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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 ...