Paid Research Panel for Customer Service Workers - West Covina, CA
Participants will share opinions through online surveys, video focus groups, and product testing. They will provide feedback on various ads, apps, and services.
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Participants will share opinions through online surveys, video focus groups, and product testing. They will provide feedback on various ads, apps, and services.
Participants will engage in paid focus groups, online surveys, and product testing to provide feedback on various ads, apps, and services. Responsibilities include completing a profile to match with relevant studies and sharing opinions through online or video formats.
Develop and improve AI methods and systems to ensure the reliability of AI agents in production environments. Collaborate with product and engineering teams to translate research prototypes into practical, production-facing capabilities.
Selected candidates will conduct literature reviews and policy analysis on topics related to human rights, governance, and international relations. They are responsible for drafting research papers, policy briefs, and analytical reports under structured supervision.
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Selected candidates will conduct literature reviews and prepare research summaries, issue notes, and analytical briefs on policy, legal, or human rights topics. They will also draft research papers or policy reports under supervision while adhering to academic integrity and research standards.
Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. You will be responsible for completing your research profile to receive relevant study invitations.
The Research Associate is responsible for the quantification and measurement of core laboratory studies, including the review of echocardiograms and other imaging modalities. They will also participate in the development of quantification manuals and ensure adherence to industry standards and regulatory requirements.
Participate in online focus groups, surveys, and product tests to provide feedback on various services and products. Complete a profile to be matched with relevant research studies.
Conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols and regulatory requirements. Maintain communication with site staff, verify investigator qualifications, and review clinical data for accuracy and protocol adherence.
The role involves conducting site visits to ensure compliance with clinical protocols, regulatory requirements, and good clinical practice. Responsibilities also include verifying investigator qualifications, managing drug accountability, and reviewing clinical data for accuracy and safety.
Conduct qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements. Communicate with medical site staff and verify the accuracy of research documentation and patient data.
The Clinical Research Associate will conduct site visits to ensure compliance with protocols, regulatory requirements, and GCP standards. They are responsible for verifying investigator qualifications, managing investigational product accountability, and reviewing clinical data for accuracy.
Conduct pre-study, initiation, monitoring, and closeout visits for research sites in accordance with SOPs and GCP guidelines. Maintain site correspondence, manage study files, and oversee clinical research data and patient charts.
Conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols and regulatory requirements. Communicate effectively with site staff, verify investigator qualifications, and manage investigational product accountability and data reporting.
Conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols and regulatory requirements. Communicate with medical site staff to verify investigator qualifications, manage investigational product accountability, and review clinical data for accuracy.
The Site Director is responsible for the end-to-end management of clinical sites, including study start-up, monitoring, and ensuring compliance with regulatory requirements. They will oversee patient recruitment, data accuracy, and maintain strong relationships with investigators to ensure high-quality study execution.
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You will own the threat model for a decentralized training and inference network, identifying risks like poisoning and data extraction. Additionally, you will design and implement statistical verification algorithms to ensure the integrity of work performed by untrusted workers.
You will build the end-to-end RL post-training stack, including rollout ingestion, reward computation, and policy updates for decentralized hardware. Additionally, you will invent new algorithms to handle asynchronous, high-latency generation and ship the first decentralized post-trained models.
You will own the end-to-end inference stack, including pipeline-parallel execution, routing, and failure handling. Additionally, you will invent and implement novel algorithms to optimize inference on consumer hardware over the public internet.
You will build and optimize distributed training systems for large models on heterogeneous hardware across decentralized networks. This includes implementing performance optimizations, ensuring fault tolerance, and developing instrumentation for monitoring training throughput and quality.
The Senior Specialist provides non-financial pre- and post-award grants administration support to faculty and scientific staff. Responsibilities include managing grant portfolios, submitting proposals, and coordinating with various administrative departments.
Participate in voluntary paid research studies, including online or video focus groups, surveys, and at-home product tests. Share feedback on advertisements, apps, services, and products.
Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. You will be responsible for completing your research profile to ensure you are matched with relevant study opportunities.
Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. You will be responsible for completing your profile to receive relevant study invitations.
The Research Assistant will support the SMILE-TB clinical trial by implementing protocol steps and managing regulatory and trial operations across international sites. Responsibilities include collecting study data, performing data entry, and maintaining communication with study participants.
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Participants will share opinions through online or video focus groups, surveys, and product testing. They will also provide feedback on various ads, apps, and services.
The Clinical Research Associate is responsible for the site management, monitoring, and close-out of assigned clinical trials to ensure patient safety and regulatory compliance. They act as the primary point of contact for investigator sites, facilitating communication and ensuring adherence to study protocols and Good Clinical Practices.
The Clinical Research Budget Manager is responsible for developing and negotiating clinical research budgets while ensuring compliance with institutional and regulatory standards. They will collaborate with cross-functional teams to assess study feasibility and provide budgetary guidance to faculty and research staff.
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