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Build multimodal computer-use agents and post-training and evaluation systems for browser, desktop, and cross-application workflows. Create workflow-based environments, rewards, and experiments, then assess and deploy improvements while ensuring reliable recovery, completion, and safe boundary enforcement.
Own the development of open-source reinforcement learning, environment, evaluation, and agent systems, and build researcher-facing features for Prime's training platform. Work with external researchers and contributors to create stable interfaces, technical resources, and a coherent path from task design through evaluation, training, and deployment.
Build simulation and real-world environments, evaluations, agent systems, and post-training methods for long-horizon robotics tasks. Train and assess embodied agents using reinforcement learning and other methods, and improve their ability to adapt, recover, and operate safely under real-world constraints.
Build quantitative research environments, agents, evaluations, and post-training methods for systematic decision-making in finance. Develop realistic simulations and production feedback loops, and assess whether results are robust across data, market regimes, risk constraints, and infrastructure.
Build and deploy post-training and agent systems for public-sector and regulated-industry partners, including private improvement loops, permissioned agents, and high-assurance evaluations. Run experiments within partner data and infrastructure constraints, assess results against meaningful baselines, and turn reusable findings into research, open-source systems, and product capabilities.
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Lead applied reinforcement learning programs from customer discovery through environment and evaluation design, post-training experiments, deployment, and measurement of practical outcomes. Identify which components drive results and turn reusable findings into shared research, open-source systems, and product capabilities.
Participate in paid online or video focus groups, surveys, and at-home product tests. Share feedback on advertisements, apps, services, and other products.
Review and support the development and submission of compliant research proposals, including budgets, required approvals, subcontractor documentation, and sponsor-specific submission requirements. Review and set up awards, support ongoing project administration and sponsor communications, process award changes and approvals, and coordinate project closeout.
Manage day-to-day clinical trial activities, including participant recruitment, screening, enrollment, consent, study visits, protocol procedures, and retention. Prepare study documents, monitor participant safety, document study data, report adverse events, and coordinate financial reconciliation and trial closeout with investigators, sponsors, and hospital departments.
Research and resolve client inquiries and disputed claims by investigating claims data, system configuration, processing, and contractual issues. Prepare client reports, collaborate across departments to address operational issues and trends, and recommend process improvements.
Support research leads in managing multiple quantitative market research projects, from questionnaire development and survey testing through fielding, data quality checks, and analysis. Develop coding frameworks, review tabulations, identify findings, and produce accurate PowerPoint reports and other research deliverables.
Lead research and design evaluations and audit methods for frontier AI systems, including pilot audits, reproducible testing pipelines, and rigorous reports with actionable recommendations. Collaborate across research, engineering, policy, and standards teams, publish findings, and handle confidential information appropriately; at the Director level, set the research agenda and represent AVERI externally.
Create realistic Excel modeling tasks based on investment banking, credit, and research work, including extending, repairing, or building models. Complete each task to establish the correct result, then develop precise yes-or-no grading criteria for AI model attempts.
Support the Principal Investigator and study team by coordinating research activities, managing study cohorts, and collecting, managing, analyzing, and reporting data. Assist with epidemiological and population-based studies, including subject outreach, mailings, follow-up, and obtaining required documents.
Identify where voice models fall short, define measurable improvement targets, and design evaluations to determine whether models improve and why. Curate or generate data, fine-tune models, build working systems, and ship customer-facing improvements to production.
Identify customer-facing shortcomings in voice models, define measurable improvement targets, and design evaluations to determine whether models improve. Curate or generate data, fine-tune models, build working systems, and ship improvements to production.
Conduct clinical trial monitoring at assigned oncology and hematology sites, from feasibility and study start-up through recruitment, routine monitoring, and closeout, in compliance with ICH-GCP, local regulations, and company procedures. Track site performance and study milestones, maintain inspection readiness, communicate progress and issues, and identify quality gaps and corrective actions in collaboration with clinical operations teams.
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Assist the principal investigator with data analysis, literature reviews, and development of models concerning polyphosphate storage in marine phytoplankton. Attend weekly meetings to set objectives and review progress, and perform other duties as assigned.
The Senior Research Analyst will produce in-depth research on the robotics value chain to define the firm's investment views and market authority. They will also support the investment team with due diligence and represent the firm externally through public-facing analysis.
The Regional Research Director leads a team of managers to drive research, innovation, and academic collaboration strategies across Europe. They are responsible for securing research funding, managing high-impact partnerships, and engaging with executive stakeholders to advance scientific and business objectives.
Participants will share opinions through online surveys, video focus groups, and product testing. They will also provide feedback on various ads, apps, and services.
Manage clinical research activities at investigative sites from site selection and study start-up through monitoring and closeout. Train and support site personnel, oversee compliance and safety reporting, and collaborate with sites and study teams to ensure data quality and successful study delivery.
The Senior Clinical Research Associate will oversee monitoring activities at investigator sites to ensure clinical trial quality, data integrity, and regulatory compliance. They will collaborate with site personnel and project teams to support study execution and maintain inspection readiness.
Support the clinical team in scientific aspects of global development programs, including risk/benefit assessments and the preparation of key clinical documentation. Act as a subject matter expert to interface with internal and external stakeholders while contributing to innovative trial designs and post-registration life-cycle management.
The Senior Clinical Research Associate will coordinate all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They will also provide mentorship to junior team members and collaborate with cross-functional teams to implement study plans effectively.
The Medical Research Consultant provides central research coordination for the Medical Affairs department by conducting comprehensive literature searches and systematic reviews. They synthesize research findings to support the development and revision of Local Coverage Determinations (LCDs) and collaborate with interdisciplinary teams to provide actionable clinical insights.
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Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. The role involves completing a profile to be matched with relevant research studies.
The Associate Clinical Research Monitor oversees clinical research activities at investigational sites to ensure compliance with protocols, regulatory standards, and patient safety. They conduct onsite and remote monitoring visits, manage site documentation, and serve as the primary point of contact for study personnel.
The Research Manager will plan and coordinate complex research projects, ensuring delivery against agreed priorities and timelines. They are responsible for improving internal processes, prototyping automation tools, and facilitating cross-functional collaboration to unblock work.
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