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Manage and independently monitor Phase II–IV clinical trials for biotech sponsors in the Netherlands to ensure regulatory compliance. Coordinate site visits, manage study documentation, and collaborate with cross-functional teams to ensure patient safety and data quality.
Conduct quantitative and qualitative research and evaluation studies to support university educational programs. Design evaluation plans, manage complex datasets, and produce actionable reports and visualizations for stakeholders.
Drive core research initiatives to develop real-time video processing and deepfake detection technologies. Collaborate with engineering teams to translate machine learning models into production-ready product solutions.
The coordinator ensures compliance with research protocols, federal regulations, and ICH-GCP guidelines through internal monitoring and data review. They are also responsible for developing training programs and providing educational opportunities for clinical research associates.
Support a large-scale systematic literature review project by screening literature and extracting data. Assist in assessing study quality and contributing to the development of reports.
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Leads project teams to achieve goals on time and within budget by managing scope, timelines, and stakeholders. Responsible for risk management, budget tracking, and coordinating with IT functional leadership.
The Research Assistant supports health and nutrition projects through data collection, management, and fieldwork. Key duties include conducting surveys, preparing reports, and coordinating with government agencies and community stakeholders.
The role focuses on building and optimizing models that evolve in real-time through cross-stack collaboration across software, hardware, and algorithms. The scientist will drive innovation to create intelligent systems capable of efficient real-world interaction.
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
Responsible for site management, monitoring, and close-out of clinical trials to ensure patient safety and quality execution. Acts as the primary point of contact for investigator sites and ensures compliance with GCP and client standards.
Support a large-scale systematic literature review project by screening literature and extracting data. Assist in assessing study quality and contributing to the development of final reports.
Support a large-scale systematic literature review project by screening literature and extracting data. Assist in assessing study quality and contributing to the development of final reports.
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
Lead and oversee clinical trial activities at a country or regional level, focusing on remote oversight, mentorship, and quality execution. Coordinate cross-functional teams to ensure compliance, data integrity, and timely delivery of project milestones.
Manage all aspects of site management from selection to close-out for complex Phase I-III clinical trials. Provide support through training and mentoring new employees and act as a subject matter expert in customer-specific working groups.
Lead innovation and process development for high-voltage dry-type bushing technology in HVDC power transmission systems. Focus on optimizing manufacturing workflows, improving insulation materials, and enhancing production for applications up to ±800kV DC.
Support all phases of quantitative and qualitative research projects, from design and data analysis to delivering story-driven reports. Leverage AI tools to streamline workflows and partner with operations teams to meet stringent project timelines.
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Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Assist lead researchers in creating detailed investigative reports for commercial real estate loan transactions. Use public records and proprietary data to mitigate financial, regulatory, and reputational risks.
Partner with AI research and engineering leadership to define and execute hiring strategies for world-class research teams. Lead full-cycle recruiting for specialized AI talent across academia and industry while refining technical interview processes.
Conduct cutting-edge research on frontier LLMs, embedding models, and rerankers to improve unstructured data search. Innovate within the LLM agent paradigm and collaborate with research engineers to deploy models into production.
The role involves developing study protocols, conducting statistical analyses, and managing research data to support human performance objectives for USAFSAM/FESP. The expert will also prepare scientific reports and coordinate with multidisciplinary teams to disseminate research findings.
Conduct open-ended qualitative research across social media platforms to identify emerging narratives and audience attitudes. Synthesize these findings into actionable insights and deliverables for non-technical audiences.
The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.
Lead complex evidence synthesis projects by developing protocols, technical reports, and statistical analysis plans. Manage client communications and provide mentorship and oversight to junior research staff.
The Senior CRA is responsible for conducting onsite monitoring visits and managing relationships with clinical sites and investigators. They ensure data compliance, subject safety, and the adherence of clinical research projects to timelines and standards.
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Design and scale machine learning solutions to enhance personalization and member experiences at Netflix. Collaborate with cross-functional teams to move algorithms from concept to production in large-scale real-time systems.
Conduct primary and secondary market research to analyze healthcare trends, consumer behaviors, and competitor activity. Translate complex data into strategic insights and dashboards to support insurance product development and business planning.
The adjunct professor will lead one section of the Legal Research Foundations course for approximately 20 students. Responsibilities include teaching foundational research skills and conducting formative and summative assessments.
Lead and execute HEOR and real-world evidence projects in collaboration with external pharma and academic partners. Develop analytical infrastructure and translate complex research into actionable clinical insights.
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