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Charing Cross
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0 Part Time API jobs in Charing Cross, Central London + 30 miles
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You possess deep domain knowledge in language models and generative AI model architectures, including fine-tuning techniques beyond API-level implementation.
You possess deep domain knowledge in language models and generative AI model architectures, including fine-tuning techniques beyond API-level implementation.
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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 ...
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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 ...
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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
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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 ...
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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.
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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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Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling. Clinical Trial Managers with expertise in Immunology and Infectious Diseases are welcome to continue to work in their area of expertise. * Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; * Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables - 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 provide remote flexibility only with relevant experience (after probation).
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Manager, Translational Biomarker Data Pathways and Re-use
Manager, Translational Biomarker Data Pathways and Re-use
GlaxoSmithKline
Stevenage, Hertfordshire
Competitive
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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.
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Pharmaron is seeking a Director Translational Pharmacology to lead and build our disease and quantitative translational pharmacology strategy across Integrated Drug Discovery (IDD). * Define and lead Pharmarons translational pharmacology and disease strategy across therapeutic areas and modalities * Provide expert leadership in disease biology, translational science and quantitative pharmacology * PhD in Pharmacology, Biological Sciences or related discipline (or equivalent experience) * Proven leadership in translational pharmacology and disease modelling through to candidate nomination * Deep expertise in translational pharmacology, disease biology and quantitative data analysis * Shape and lead translational pharmacology strategy within a global CRO - Job Introduction - Location: UK (Hybrid) This is a pivotal leadership role, combining deep scientific expertise, strategic influence, and client ...
Pharmaron is seeking a Director Translational Pharmacology to lead and build our disease and quantitative translational pharmacology strategy across Integrated Drug Discovery (IDD). * Define and lead Pharmarons translational pharmacology and disease strategy across therapeutic areas and modalities * Provide expert leadership in disease biology, translational science and quantitative pharmacology * PhD in Pharmacology, Biological Sciences or related discipline (or equivalent experience) * Proven leadership in translational pharmacology and disease modelling through to candidate nomination * Deep expertise in translational pharmacology, disease biology and quantitative data analysis * Shape and lead translational pharmacology strategy within a global CRO - Job Introduction - Location: UK (Hybrid) This is a pivotal leadership role, combining deep scientific expertise, strategic influence, and client ...
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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.
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Learn more at are searching for the best talent for Manager, Medical Writing, Immunology. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is recruiting for a Manager, Regulatory Medical, Immunology. * If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team. * At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required. Medical Writing * Actively participate in medical writing and cross-functional meetings. * Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the work of other medical writers, external contractors, and document specialists supporting a project. * May represent Medical Writing department in industry standards working groups.
Learn more at are searching for the best talent for Manager, Medical Writing, Immunology. Purpose: Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team is recruiting for a Manager, Regulatory Medical, Immunology. * If a lead writer for a program: Primary point of contact and champion for medical writing activities for the clinical team. * At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience is required. Medical Writing * Actively participate in medical writing and cross-functional meetings. * Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed; may oversee the work of other medical writers, external contractors, and document specialists supporting a project. * May represent Medical Writing department in industry standards working groups.
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We have a great opportunity for a dynamic and motivated Hydrogeologist specialising in contaminated land and brownfield development and/or engineering hydrogeology or to join our Sustainable Land and Resource Management Practice. Overview - Transform our Urban Legacy. Based in either our Exeter, Bristol, Birmingham, Cambridge, Epsom or London office (with flexible hybrid working), you will be part of an award-winning group of hydrogeology and contaminated land experts delivering innovative brownfield solutions to major UK infrastructure projects, across the transportation, energy, buildings and places and water markets. This is a fantastic opportunity to work alongside industry leaders, contribute to high-profile UK and international projects, and grow your career in a supportive, collaborative, multi-disciplinary environment. Your Role
We have a great opportunity for a dynamic and motivated Hydrogeologist specialising in contaminated land and brownfield development and/or engineering hydrogeology or to join our Sustainable Land and Resource Management Practice. Overview - Transform our Urban Legacy. Based in either our Exeter, Bristol, Birmingham, Cambridge, Epsom or London office (with flexible hybrid working), you will be part of an award-winning group of hydrogeology and contaminated land experts delivering innovative brownfield solutions to major UK infrastructure projects, across the transportation, energy, buildings and places and water markets. This is a fantastic opportunity to work alongside industry leaders, contribute to high-profile UK and international projects, and grow your career in a supportive, collaborative, multi-disciplinary environment. Your Role
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We're looking for a Senior Development Scientist to join our client's team and help shape the next generation of protein science. Are you a protein scientist with a passion for translating cutting-edge biology into real-world products? * Apply protein characterisation techniques - such as HPLC/FPLC, mass spectrometry, or related analytical methods - to inform and accelerate product development You'll lead the design and optimisation of protein-based assays and workflows - from early feasibility through to robust, scalable solutions ready for commercial deployment. Drawing on your expertise in protein characterisation, you'll generate high-quality, well-controlled data that drives strategic decisions and moves prototypes into reliable, reproducible platform-integrated tools. * Lead and mentor a team of scientists, providing day-to-day technical guidance and line management
We're looking for a Senior Development Scientist to join our client's team and help shape the next generation of protein science. Are you a protein scientist with a passion for translating cutting-edge biology into real-world products? * Apply protein characterisation techniques - such as HPLC/FPLC, mass spectrometry, or related analytical methods - to inform and accelerate product development You'll lead the design and optimisation of protein-based assays and workflows - from early feasibility through to robust, scalable solutions ready for commercial deployment. Drawing on your expertise in protein characterisation, you'll generate high-quality, well-controlled data that drives strategic decisions and moves prototypes into reliable, reproducible platform-integrated tools. * Lead and mentor a team of scientists, providing day-to-day technical guidance and line management
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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 ...
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;