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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.
2 exact matches jobs are outside your preferred location
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Protein Function Development Team Leader
Protein Function Development Team Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
From £89,499 to £114,027 per annum
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
Overview - We are seeking an exceptional candidate for the EMBL-EBI Faculty role of Protein Function Development Team Leader, to be responsible for leading the engineering and bioinformatics infrastructure that underpins one of the most important resources in the life sciences, Uniprot. UniProt is the world's leading resource for protein sequences and functional annotation, used by hundreds of thousands of researchers globally every day. It provides comprehensive annotations across an ever-growing number of proteomes spanning the tree of life, integrating experimentally determined functional data from the literature with state-of-the-art computational predictions and richly interconnected data from partner resources. As the demands on UniProt continue to grow, in data volume, annotation depth, and the diversity of research applications it supports, a robust and ...
NEWPREMIUM
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
Familiarity with database management tools and techniques (e.g., SQL, Selenium, S3, Sagemaker, API protocols) is preferred but not required.
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FEATURED
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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
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InterPro/Pfam Software Project Leader
EMBL-EBI
Hinxton, Saffron Walden (CB10), CB10 1SA
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PREMIUM
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Head of R&D - Sensing Science
Head of R&D - Sensing Science
KO2 Embedded Recruitment Solutions LTD
Heathway, Dagenham (RM10), RM9 5AQ
£80000 - £90000 per annum
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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.
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
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - 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. * Psychiatry
We are seeking several Pharmaceutical Physicians to join our dynamic team in London. The Pharmaceutical Physician will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. The Pharmaceutical Physician will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required. All Physicians have hybrid WFH flexibility. * Previous experience in pharmaceutical-related clinical research is preferred. We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Job Summary - 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. * Psychiatry
The Senior Statistical Programmer is responsible for providing hands-on support and technical guidance on clinical study teams. The development of study and ad hoc output, including, but not limited to: ADaM datasets, tables, figures, and listings output and/or QC of requested output, is the - The main focus of this role. This individual, working closely with the study statistician, will be responsible for review and acceptance of contract research organization (CRO) deliverables, which are mainly, but not limited to, datasets in submission-ready standard format (ADaM), tables, figures, and listings, and submission packages. This individual will participate in the design, development, and quality control process for SAS programs used to access, extract, transform, review, analyze, and submit clinical data for all requested analyses.
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