applications, digital) etc. 10 - 12+ years of experience in Technology and/or Architectural consulting. Formative experiences in architecture, software engineering, data, and analytics. Pharmaceutical, Biotech or similarly regulated environment experience desirable. Must have hands-on experience in leading, managing, or overseeing core development project(s) and engineering teams. Must More ❯
product performance, roadmap, and future plans. Industry Thought Leadership: Stay abreast of industry trends, best practices, and emerging technologies in the protein design and pharma tech space. Share insights and act as a thought leader within the organization and industry events External Collaboration Leadership: Identify, initiate, and manger strategic collaborations More ❯
Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. More ❯
various relevant Microsoft platforms, tools, technologies, patterns, and techniques related to Azure tools, integration, and data is required. Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred. Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. More ❯
innovations, positioning them within broader industry trends to inform internal teams and external stakeholders. Lead simultaneous client facing projects across ZS Discovery to reinvent pharmaceutical discovery, elucidate complex disease biology and pioneer novel therapeutics. Provide expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics More ❯
london, south east england, united kingdom Hybrid / WFH Options
Proclinical Staffing
team player capable of managing multiple activities. Excellent communication, influencing, and negotiating skills. Ability to analyze business processes and design improvements. Experience in healthcare, pharma, or medical device industry is a plus. Ability to read and debug ABAP code. Experience with SAP API's and integration middleware. Bachelor's Degree More ❯
Medpace Overview 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. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We More ❯
clearly demonstrated. Industry/domain skills: Extensive expertise in finance, HR, sales, marketing, product lifecycle management, manufacturing and post-sales service. Medical device or pharmaceutical industry experience is preferred. Experience in and understanding of a wide variety of analytical processes (governance, measurement, etc.). Experience with agile software development. A More ❯
strong background in programme and project management, stakeholder engagement, and the ability to work across multiple teams to drive successful outcomes. Experience in the pharmaceutical industry or another regulated sector would be an advantage. Responsibilities: Programme Management: Lead and manage multiple projects, ensuring alignment with strategic business goals and objectives. More ❯
chat. The AI/ML Clinical Development team is responsible for creating AI/ML applications to support the development of GSK's assets (Pharma and Vaccine), from early to later-stage development, aligned with GSK's strategy of "software for every asset." Solutions range from response prediction to complex More ❯
headquartered in Menlo Park, California, with locations in Washington, D.C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. GRAIL is looking for a full-stack Senior Software Engineer to join its clinical software team based in our London office. More ❯
London, England, United Kingdom Hybrid / WFH Options
Pear Bio
deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis and machine learning. Experience working with high More ❯
london, south east england, United Kingdom Hybrid / WFH Options
Pear Bio
deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis and machine learning. Experience working with high More ❯
relevant professional experience. Qualification: Extensive experience in delivering Enterprise level SAP Finance and controlling solutions including S/4 experience, with strong preference for pharmaceutical industry experience. Proficiency in SAP Cost Accounting configuration and testing in all major areas. Professional certifications (SAP FICO, PMP, CMA, etc.) are a plus. Familiarity More ❯
Job Description Senior Information Security Analyst Our Client is a leading global company specialising in pharma products. They are looking to recruit a Senior Information Security Analyst with at least 5 to 7 years expertise in Technology Security. The Senior Information Security Analyst is responsible for maintaining information security policies More ❯
Experience : A minimum of 8 years of relevant work experience; a minimum of 6 years relevant SAP experience; a minimum of 4 years relevant Pharma experience. Domain Expertise Deep End-to-End understanding of Supply Chain Finance and Intercompany business processes, such as: Sourcing of direct Materials, Subcontracting Processes, Toll More ❯
in AI/ML and mechanistic modeling (designing, developing and maintaining both mechanistic and data driven products for in-silico running of R&D pharma laboratory experiments). Experience in partnering with R&D labs domain (Pre-Clinical and CMC) and in the digitalization of technical process development through modeling More ❯
Profibus, Modbus, DeviceNet). Knowledge of process instrumentation and wiring would be desirable. Experience working with validated Digital Manufacturing/Automation systems in the Pharmaceutical or Food Beverage manufacturing environment. Characteristics We look for candidates who Work well as part of a team. Have excellent problem solving and diagnostic skills. More ❯
company, is leading the digital transformation of life sciences, creating hope for millions of people. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 2,000+ More ❯
Life Sciences with a compelling value proposition - building on Veeva's position as the digital partner of choice for 85% of the top 20 Pharmaceutical companies. As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers - managing teams and planning, organizing, and tracking all aspects More ❯
academic record in business, medical or life sciences, engineering, applied math, statistics or related fields. Alternately, candidates may possess a Masters (preferably PhD) in pharmaceutical sciences, decision sciences or related field with a business application. 4-8 years of relevant post-collegiate job experience. High motivation, good work ethic, maturity More ❯
You will need to login before you can apply for a job. View more categories View less categories Sector Science and Pharmaceutical ,Technology Role Senior Executive Contract Type Permanent Hours Full Time DESCRIPTION Are you interested in shaping the future of movies and television? Do you want to define the More ❯
on engineering excellence and unrivalled commitment to customer service is trusted by the most important organisations across the UK and Europe in the technology, pharmaceutical, financial, and e-commerce industries. We're proud to have earned one of the best reputations in the industry, and it is essential to us More ❯
often Preferred qualifications: Demonstrated experience of Python backend development (e.g. using FastAPI) Demonstrated experience with biological or scientific data (e.g. genomics, transcriptomics, proteomics), or pharmaceutical industry experience Knowledge of AI/ML approaches and deployment of AI/ML powered applications - especially using language models or NLP and agent-based More ❯
management systems (EDMS). Experience required: Degree in Life Sciences, Information Technology, Regulatory Affairs, or related field Extensive experience in regulatory operations within the pharmaceutical industry Proficiency in Veeva Vault RIM Suite, eCTD management systems, and other regulatory systems Strong analytical, problem-solving, and decision-making abilities Understanding of Electronic More ❯