Date posted
Commute time
Locations
Type of Company
Job types
Locations
Locations
Date posted
Type of Company
Job types
Locations
There is no job matching your search
Api
Surrey
No need to fret! We’re adding new jobs every single day. Find out immediately when we’ve found a match for you.
2 exact matches jobs are outside your preferred location
)
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.
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
NEW
These jobs might also interest you
)
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in Endocrinology / Metabolic related areas, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system - Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
)
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 ...
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 ...
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency. Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering team. * Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and * Bachelors in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; * Clinical research experience is preferred;
)
The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
The Medical Affairs Director UK is a key member of the Country DPS Board, acting as a strategic partner to the business. Medical Affairs Group Medical Affairs * Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs. * Experience in research and/or industry roles (Medical Affairs, Clinical, or R&D) within a highly regulated pharmaceutical or medical device environment. Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Consulting, Customer Analytics, Design Mindset, Digital Culture, Digital Literacy, Healthcare Trends, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Strategic Thinking, Tactical Thinking, Technical Credibility * Build and maintain strong external relationships with key stakeholders, including ...
NEW
)
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.
)
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
A top tier consultancy firm is currently seeking an experienced Data Scientist to join a dynamic team focused on leveraging Large Language Models (LLMs) and advanced machine learning to drive tangible business value. As a Data Scientist, you will act as the technical architect behind our AI solutions. If you are an experienced data scientist looking for a new exciting challenging role then this could be the perfect opportunity for you. * Build pipelines that gather and clean data, making sure everything used to train the AI is accurate and high-quality. When things could be better, tweak the settings or data to boost accuracy and efficiency. 12 Months Contract Inside IR35?? London - 2 days a week in the office?? £500 a day - This is a pivotal role where you will take ownership of the end-to-end model lifecycle-from initial conceptualisation and prompt engineering to production deployment.
FEATURED
)
SF Technology Partners are working with a Private Equity backed property operations business based in London who are looking to appoint a highly skilled Principal Data Scientist, focused on improving, automating and driving efficiency in the existing finance processes, as the business looks to modernise. You will be given the autonomy to partner with key business stakeholders and be expected to quickly understand the existing processes and procedures in place, before utilising a highly analytical data driven approach to design, plan and execute significant process upgrades across the Finance function in conjunction with the CFO. You will be expected to lean on demonstrable skills in API Integrations, automation scripting & RPA as well as to effectively use Python, SQL & other big data tools to optimize existing processes, ensuring more efficient working ...
SF Technology Partners are working with a Private Equity backed property operations business based in London who are looking to appoint a highly skilled Principal Data Scientist, focused on improving, automating and driving efficiency in the existing finance processes, as the business looks to modernise. You will be given the autonomy to partner with key business stakeholders and be expected to quickly understand the existing processes and procedures in place, before utilising a highly analytical data driven approach to design, plan and execute significant process upgrades across the Finance function in conjunction with the CFO. You will be expected to lean on demonstrable skills in API Integrations, automation scripting & RPA as well as to effectively use Python, SQL & other big data tools to optimize existing processes, ensuring more efficient working ...
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 ...
)
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
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine, medical physics, medical imaging / radiopharmaceuticals or / radiation oncology for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. * Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM). * Compile and maintain project-specific status reports within the clinical trial management system
Medpace is 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 ...
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 ...
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 ...
)
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
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;
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
)
We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
We are seeking an experienced Data Scientist with strong Data Engineering capabilities to support the Digital Screening programme. Role: Data Scientist / Engineer - You will work within a multidisciplinary Agile team, collaborating with Data Engineers, Analysts, and User-Centred Design (UCD) professionals to deliver robust, data-driven insights and scalable data solutions. * Lead exploratory data analysis (EDA) to inform dashboard design and reporting outputs * Define data requirements and determine appropriate dashboard content * Identify and mitigate data quality risks and ensure data integrity * Design, build, and maintain reusable data pipelines and datasets using Python and PySpark * Work with stakeholders to translate business needs into data solutions and insights * Solid background in exploratory data analysis and data modelling
NEWFEATURED
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;
)
Director, Regional Ecosystem Lead (Northern Europe & UK)
Director, Regional Ecosystem Lead (Northern Europe & UK)
CSL Behring
Fishery, Maidenhead (SL6), SL6 1PT
Competitive
Could you be our next Director, Regional Ecosystem Lead (Northern Europe & UK). Partner closely with TA Search Leads to conduct regional searches, plan engagements and conferences, and share regional insights and updates.? Serve as the key CSL leader within the regional innovation ecosystem, actively sourcing opportunities aligned with all TA strategies and portfolio priorities. Serve as a senior member of deal teams occurring in each region, supporting transactions from identification through due diligence and help lead relationships with external partners through deal close.? Provide insights on regional biotech trends, competitive landscape, and innovation hotspots. 10+ years in biopharma, external innovation, or business development with strong regional network and ecosystem knowledge.? Proven ability to source and evaluate external opportunities and lead deal execution.?
Could you be our next Director, Regional Ecosystem Lead (Northern Europe & UK). Partner closely with TA Search Leads to conduct regional searches, plan engagements and conferences, and share regional insights and updates.? Serve as the key CSL leader within the regional innovation ecosystem, actively sourcing opportunities aligned with all TA strategies and portfolio priorities. Serve as a senior member of deal teams occurring in each region, supporting transactions from identification through due diligence and help lead relationships with external partners through deal close.? Provide insights on regional biotech trends, competitive landscape, and innovation hotspots. 10+ years in biopharma, external innovation, or business development with strong regional network and ecosystem knowledge.? Proven ability to source and evaluate external opportunities and lead deal execution.?
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Biostatistics and Statistical Programming Operations - The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions * Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews.
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. * Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. * Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) * Biostatistics and Statistical Programming Operations - The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program. ( Positions available supporting multiple Therapeutic Areas available ) Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions * Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews.
Datatech Analytics is partnering with a leading global consultancy to hire Data Science Consultants into a growing Digital & Data practice delivering advanced analytics, AI and modelling solutions across complex, real-world environments. This is an opportunity to work on projects where data science directly influences operational performance, strategy and decision making across sectors including financial services, defence, government, energy, healthcare and consumer markets. You'll join multidisciplinary teams spanning data science, engineering, analytics and consulting, helping clients move from raw data and business problems through to deployable insight and measurable outcomes. You'll work across the full data science lifecycle, partnering closely with clients and delivery teams to build analytical solutions that drive commercial and operational impact.
Datatech Analytics is partnering with a leading global consultancy to hire Data Science Consultants into a growing Digital & Data practice delivering advanced analytics, AI and modelling solutions across complex, real-world environments. This is an opportunity to work on projects where data science directly influences operational performance, strategy and decision making across sectors including financial services, defence, government, energy, healthcare and consumer markets. You'll join multidisciplinary teams spanning data science, engineering, analytics and consulting, helping clients move from raw data and business problems through to deployable insight and measurable outcomes. You'll work across the full data science lifecycle, partnering closely with clients and delivery teams to build analytical solutions that drive commercial and operational impact.
)
R&D Actuarial Analyst
R&D Actuarial Analyst
Vitality Corporate Services Limited
Charing Cross, Central London (WC2), WC2R
£Competitive + Bonus + Benefits
This role suits a well-rounded actuarial analyst who is curious about behaviour, passionate about wellness, confident with stakeholders and motivated by seeing their analysis drive real outcomes. Team Enterprise R&D * Apply actuarial techniques to assess impacts on mortality, morbidity and persistency * Experience supporting pricing, product evaluation or actuarial analysis * Understanding of key actuarial concepts including mortality, morbidity and persistency * Experience with Python or R for data analysis - About The Role - Working Pattern - Hybrid 2days per week in the Vitality London Office. Full time, 37.5 hours per week. We are happy to discuss flexible working! * Demonstrated data-driven insight * Excellent written and verbal communication skills * Product and behavioural thinking experience - What this role is all about - The role will support research, idea generation and product development across the ...
This role suits a well-rounded actuarial analyst who is curious about behaviour, passionate about wellness, confident with stakeholders and motivated by seeing their analysis drive real outcomes. Team Enterprise R&D * Apply actuarial techniques to assess impacts on mortality, morbidity and persistency * Experience supporting pricing, product evaluation or actuarial analysis * Understanding of key actuarial concepts including mortality, morbidity and persistency * Experience with Python or R for data analysis - About The Role - Working Pattern - Hybrid 2days per week in the Vitality London Office. Full time, 37.5 hours per week. We are happy to discuss flexible working! * Demonstrated data-driven insight * Excellent written and verbal communication skills * Product and behavioural thinking experience - What this role is all about - The role will support research, idea generation and product development across the ...
PREMIUM