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Certifications such as Microsoft Certified: Azure Developer Associate, Certified Software Development Professional (CSDP), Certified Secure Software Lifecycle Professional, or similar is preferred.
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Excellent technical skills with proven ability to manage databases, perform web scraping, and leverage coding for report automation. This position is a member of the Gas Market Analytics team which is responsible for market analysis, developing fundamental market models, short and long term balance and price forecasting using statistical and qualitative methodologies in support of gas and power trading activities.
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Join our growing Medical Affair team in the role of Associate Director, Outcomes Research & RWE. Your expertise will play a pivotal role in advancing real-world evidence and value development and integrated medical affair plans at Taiho.
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Develop software applications and systems used by the R&D Organization and provide application solutions tailored for R&D functions such as Research Informatics, SDMS (Scientific Data Management System), Lab Management Systems, Lab and Data Integrations, Research Data products, Pathology, Imaging, Pharmacology, Development Operations etc.
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Preparing and executing CMC regulatory development strategies in biologics, experience leading successful NDA/BLA submission required, drug delivery device experience preferred. Provides input into CMC regulatory strategies: define regulatory pathways and milestones for submissions to support development activities leading to successful NDA/BLA approvals.
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Use of platforms in content management systems, such as Wordpress and Drupal; design and editing software, such as Adobe Creative Suite (Photoshop, Illustrator, InDesign, and Acrobat); and CRM tools such as Mailchimp.
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Experience in creating and maintaining electronic media; e.g., web pages (Drupal), online training (Captivate, Storyline) The successful candidate will be responsible for developing thorough knowledge of all applicable standards, codes and regulations; providing timely dissemination of pertinent information to all segments of the University; developing and presenting training with minimal direction from senior EHS staff; developing and maintaining web-based materials in support of assigned programs, fielding technical questions, and providing health and safety consultation as needed.
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Knowledge of CMC regulatory requirements for advanced therapies and/or biologics during development and post-approval. Provide strategic CMC regulatory expertise for development project teamsProvide strategic input to development & GO teams to mitigate drug supply issues.
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As a member of the team, you will contribute to the research, design, development and maintenance of low-latency, distributed web scraping solutions. Bloomberg Data Technologies Engineering is seeking a Senior Software Engineer that has a passion for full stack development, design/implementation skills, and experience integrating multiple external and internal systems.
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While this position is primarily focused on statistical methods research and development, it also involves close collaboration with the Study Design Innovation and Optimization (StuDIO) function within Global Biometrics and Data Sciences of BMS. StuDIO’s mission is to support and enable development teams to pursue optimal design/development options with sharpened focus on scientific rigor and innovation, operational feasibility, and resource efficiency across the BMS portfolio.
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Methodology: Knowledge of Agile software development methodology. Responsibilities Software Development and Maintenance. Qualifications Experience: At least 7+ years of hands-on experience with modern JavaScript backend and PHP development.
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Represents department in business development due diligence and partner alliance management as appropriate; sits on JDC/JRC/JSC as appropriate. Designs and develops clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies.
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The Executive Director, Clinical Development & Quality Operations is a critical management position within the R&D Quality organization that is responsible for the development and strategic oversight of the Therapeutic Area Quality, Vendor and Data Quality as well as Quality Risk Management.
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Development and implementation of comprehensive site investigations by participating in scope of work development, field work, and data analysis to characterize contaminants in sediments, soil, air, surface water, and groundwater.
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Acts as PCOR Account Lead responsible for leading company response from Deal to Contract (includes pre-deal assessment/analysis, development of business cases for Pricing Committee, offer development, contract development, negotiation, pre-deal forecasting and reporting of contract profitability of customer segments for all Novo Nordisk products (diabetes, obesity and rare disease products.
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software developer c web development jobs Company: Brilliant in Princeton, NJ
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