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Develop and execute accelerated imagery preprocessing pipelines and workflows for finetuning large geospatial vision models. Collaborate on multidisciplinary teams to advance GeoAI methods and communicate results through technical reports and peer-reviewed publications.
Own the measurement of quality for Figma's AI-powered experiences by defining quality dimensions and building evaluation frameworks. Partner with cross-functional teams to establish repeatable evaluation pipelines and provide decision-ready signals for shipping AI features.
Lead the identification and acquisition of new business opportunities within the healthcare market research sector to drive revenue growth. Manage the full sales cycle from lead generation to contract negotiation while maintaining long-term client relationships.
Conduct research using web-based media databases to produce high-quality due diligence reports on companies and individuals. Ensure report accuracy and timeliness while collaborating with senior analysts and performing watchlist screenings.
The CRA is responsible for conducting site monitoring visits and ensuring clinical trial compliance with protocols and quality standards. They provide oversight to the CRA team, manage site relationships, and ensure the integrity of CRF data through meticulous verification.
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Lead the end-to-end development and submission of NIH R01 grant applications for medical imaging research. Collaborate with internal scientists and external US-based academic and clinical partners to define scientific scope and methodology.
The Assistant Research Professor leads living systematic reviews and meta-analyses focused on school-based mental health prevention for K-12 students. They are responsible for translating research findings into accessible evidence products and coordinating new project proposals and grants.
The CRA II is responsible for monitoring Phase I-IV oncology clinical trials to ensure compliance with protocols and regulatory requirements. Key duties include conducting site visits, training personnel, and managing site activities from start-up to close-out.
Conduct comprehensive market research and sizing across various financial segments to identify high-growth opportunities. Perform customer discovery through interviews with financial executives to validate pricing and go-to-market assumptions.
Design and evaluate routing policies for LLM traffic and build agentic benchmarks to measure algorithm quality. Collaborate with engineering teams to integrate software across the NVIDIA accelerated serving stack and contribute to open-source repositories.
Serve as the primary contact between investigational sites and the sponsor while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and driving high-quality data entry.
Serve as the primary contact between investigational sites and the sponsor while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Oversee patient safety reporting, drug accountability, and high-quality data entry within CTMS and eTMF systems.
Serve as the primary contact between investigational sites and the sponsor while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and driving high-quality data entry.
The Lead CRA provides leadership and oversight to the CRA and CTA teams to ensure the accurate and timely conduct of clinical trials. They serve as the primary liaison between study sites, internal staff, and clients while managing clinical monitoring plans and quality issues.
Lead the end-to-end screening process for a global pivotal trial, ensuring accurate pre-procedure assessments and eligibility decisions. Collaborate with cardiologists and field teams to prioritize participants and ensure protocol compliance.
The specialist ensures institutional, state, and federal compliance for human and animal research by reviewing IRB/IACUC submissions and maintaining auditable records. They also coordinate education and outreach initiatives and monitor post-approval compliance to improve research operations.
The analyst ensures billing compliance for clinical research by evaluating protocols, budgets, and consent forms to create coverage analyses and study calendars. They collaborate with research teams to optimize financial workflows and ensure adherence to Medicare and other regulatory rules.
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The role involves providing technical and programmatic support to NIST's Forensic Science Research Program by documenting practices and strengthening national standards. Key tasks include facilitating process mapping working groups, auditing standards, and identifying opportunities for AI integration in forensic workflows.
Conduct groundbreaking research in generative audio focusing on vocal synthesis, post-training alignment, and audio editing. Collaborate with cross-functional teams to develop artist-first AI music products and publish findings in the research community.
The Senior Research Associate designs and executes rigorous mixed-methods research studies to demonstrate the impact of family-school partnerships on student outcomes. They manage the full research lifecycle from data collection and analysis to translating complex findings for internal and external stakeholders.
Conduct groundbreaking research in generative audio focusing on vocal synthesis, post-training alignment, and audio editing. Collaborate with cross-functional teams to develop artist-first AI music products and publish findings in the research community.
Conduct original research to advance generative AI systems for professional creative workflows across image, video, 3D, and vector graphics. Translate research insights into prototypes and model capabilities that inform product direction and improve creator workflows.
Own the product direction and roadmap for a Population Genomics Research Platform, managing the researcher experience and scaling the global user network. Coordinate with biobank stakeholders and engineering teams to deliver compliant, high-scale analytical workflows for human disease research.
Contribute to the mission of expanding clinical trials to a broader range of sites and patients globally. Work within a fast-growing startup environment to build sustainable solutions for clinical research operations.
Lead the end-to-end quantitative research process from design and implementation to delivering actionable brand strategy insights. Serve as the primary client contact and drive new business growth through the cultivation of existing and new opportunities.
Manage research activities at clinical sites, including site identification, start-up, and close-out. Ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
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Conduct standardized phone interviews to collect research data while maintaining strict confidentiality. Accurately enter gathered information into the database and perform general administrative office functions.
The role involves coordinating clinical trial visits and administering trial medications while ensuring accurate data collection in Case Report Forms. The nurse will also manage sample dispatch and report adverse events in compliance with SOPs and GCP guidelines.
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 to the site team.
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
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