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The Senior CRA is responsible for investigative site management and monitoring activities throughout the clinical trial lifecycle for Oncology trials. Key duties include ensuring data integrity, subject safety, and maintaining a continuous state of inspection readiness.
Design and execute pharmacoepidemiology studies using real-world data to address safety research questions during drug development and for marketed products. Collaborate with cross-functional teams and external stakeholders to identify evidence gaps and contribute to Integrated Evidence Generation Plans.
Analyze and forecast process technology roadmaps for DRAM, NAND, and HBM to provide differentiated research for institutional clients. Translate complex technical developments into economic implications and supply-model inputs for the semiconductor industry.
The role involves building first-principles performance models for AI accelerators and rack-scale systems to analyze inference and training workloads. The analyst will translate technical hardware characteristics into economic conclusions and TCO research for institutional clients.
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Lead the daily operations, performance, and compliance of Clinical Research Specialist staff across designated health system accounts. Serve as the primary operational liaison to ensure high-quality service delivery and maintain strong customer relationships with health system partners.
Lead technical analysis and multidisciplinary projects to develop engineering solutions for building decarbonization and energy efficiency. Conduct field studies and mentor junior staff while identifying new research and consulting opportunities to advance climate solutions.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
The Senior CRA manages communication with project stakeholders and maintains relationships with clinical sites to ensure research standards and timelines are met. Key duties include conducting onsite monitoring visits, performing data verification, and supervising study activities at the country level.
The Senior Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance for clinical research projects. They will also supervise study activities, timelines, and support regulatory document preparation for various therapeutic indications.
The role involves independently directing systematic literature review (SLR) projects, from defining research questions and designing search algorithms to synthesizing evidence. Additionally, the position requires managing project timelines, budgets, and leading client communications while overseeing junior staff.
The CRA I coordinates clinical monitoring and site management to ensure protocol and regulatory compliance. They conduct site visits, manage documentation, and maintain collaborative relationships with investigational sites to guarantee data reliability.
The CRA is responsible for managing the full lifecycle of study sites, including qualification, initiation, monitoring, and close-out. They ensure protocol adherence, verify source documents for data veracity, and provide guidance to site staff and junior CRAs.
The role involves conducting market and competitor research to identify growth opportunities and leveraging generative AI to enhance reporting and workflows. The specialist will partner with Product and Strategy teams to deliver actionable insights that shape the company's product portfolio.
The role involves assessing how frontier AI increases misuse risks in biological activity and developing safeguards and detection approaches. The resident will turn these analyses into concrete recommendations for developers, policymakers, and government partners.
Investigate and monitor emerging threats at the intersection of AI, biosecurity, and national security using open-source information. Produce decision-ready assessments on actors, capabilities, and technical trends for internal teams and external government partners.
Review and critique visual design artifacts to translate intuitive judgment into structured tasks. Develop clear evaluation rubrics to help improve AI models' understanding of visual design.
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The Research Assistant supports the design, execution, and dissemination of applied research in child welfare, juvenile justice, and behavioral health. Key duties include conducting literature reviews, analyzing data using various methodologies, and preparing findings for internal and external stakeholders.
The Research Navigator manages the protocol optimization process and end-to-end grant production for clinical research in Neurology. They serve as a liaison between investigators and leadership to ensure high-quality study design and successful funding outcomes.
Manage the full lifecycle of quantitative and qualitative research projects from proposal to delivery. Translate complex data into actionable insights and strategic recommendations for high-profile clients in entertainment and technology.
The Research Assistant oversees data collection, organization, and management for research studies. Responsibilities include running reports, cleaning data, conducting literature searches, and assisting with the preparation of publications and policy briefs.
Design and lead strategic research projects to address operational and management issues in higher education. Synthesize complex findings into actionable insights and advisory services for campus executives and leadership teams.
The Director will drive cross-functional process improvements across clinical research operations to accelerate study activation and increase patient accrual. They will act as the primary bridge between research operations and the technology team to translate process designs into automated solutions and AI tools.
Design and lead real-world evidence studies to connect health signals to outcomes, healthcare utilization, and cost savings. Collaborate with data science and external partners to produce rigorous research outputs for clinical and commercial audiences.
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The role serves as the scientific bridge between generative chemistry workflows and external partners to develop PFAS-free semiconductor materials. Key duties include running discovery workflows, ranking candidate molecules, and translating experimental feedback into technical improvements.
Drive sustainable territory growth by developing new business and expanding existing accounts within the Waters Biosciences division. Act as the strategic owner of the territory, aligning customer needs with integrated solution-based value across the portfolio.
Design and build the agent execution harness and orchestration layer to enable AI agents to reason over enterprise data and execute workflows. Lead the development of evaluation frameworks, prompt management systems, and LLM integration strategies to ensure reliability and scalability at Fortune 500 scale.
The attorney will conduct substantive legal research on complex family law issues and draft high-quality motions, pleadings, and briefs. They will also provide back-end litigation support and collaborate with the legal team on case strategy.
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