Top Research Jobs in Seattle, WA

This role involves developing AI applications, focusing on LLMs and agent frameworks, and requires research skills in ML with experience in data strategy.

Lead research in user modeling and personalization, focusing on generative and language models, recommendation and retrieval systems. Build scalable prototypes, partner with engineering to deploy solutions, mentor junior researchers and interns, and publish work at top conferences.

Leads an independent deep learning research agenda, develops original research in foundation models and related AI applications, publishes in top-tier venues, and collaborates with researchers, engineers, and product groups to translate breakthroughs into products and services.

Coordinates daily operations for investigator-initiated and industry-sponsored clinical trials. Responsibilities include screening and enrolling patients, obtaining informed consent, scheduling visits, managing study supplies and samples, maintaining regulatory and source documentation, supporting billing compliance, coordinating monitoring visits, entering data, and serving as a liaison among patients, providers, and research teams. The role requires adherence to study protocols, Good Clinical Practice, and applicable regulatory requirements.

Design, optimize, and deploy large language model training and post-training pipelines. Improve model quality through fine-tuning, reinforcement learning, preference optimization, evaluation, and experimentation. Build PyTorch-based infrastructure, optimize distributed multi-GPU training, diagnose performance and convergence issues, and develop production-ready AI systems. Collaborate with researchers, infrastructure engineers, platform teams, and customers while contributing to open-source projects and reusable training capabilities.

Develop and post-train deep learning models while building systems, tooling, and workflows for training, evaluation, debugging, and deployment. Contribute to open-source projects, distributed AI infrastructure, backend services, and developer platforms. Collaborate with research, product, infrastructure, and customer teams to solve complex technical problems, prototype ideas, and productionize successful experiments.

Organize and curate large volumes of raw information: extract key points from transcripts, maintain clean spreadsheets, curate links/resources, tag and categorize content, and follow or propose systems for information structure. Part-time remote role with initial 10 hours/week and potential to grow.

Research and forecast memory process-technology roadmaps (DRAM, NAND, HBM), evaluate manufacturing integration and economics, map technology transitions to equipment demand, benchmark vendor execution, translate technical disclosures into actionable research, and contribute to industry models and client-facing publications.

Lead forward-looking research on robot learning, hardware, supply chains, and commercialization. Produce reports, forecasts, and briefings; track mobile manipulators, quadrupeds, cobots, and autonomous vehicles; assess AI, edge compute, and simulation impacts; collaborate with cross-sector analysts; support investors, OEMs, and policy stakeholders; and present findings to senior executives and clients.

Conduct China-focused semiconductor and AI supply-chain research, produce data-rich equity notes and weekly coverage, build bottoms-up financial models for Chinese foundries, fabless designers, memory and equipment firms, monitor disclosures and policy, engage industry contacts, and support institutional clients with timely analysis.

Leads primary and secondary market research, business analytics, and competitive intelligence supporting lorundrostat’s commercial planning and launch. Develops strategic frameworks, manages research vendors and data providers, monitors competitors, supports forecasting and market access planning, answers commercial and epidemiological questions, and provides insights for leadership, investor, and board presentations. The role also manages the business insights budget and requires expertise in U.S. pharmaceutical markets, commercial data sources, payer environments, and clinical trial evaluation.

Provides clinical research nursing support for cellular immunotherapy and autoimmune studies. Responsibilities include participant advocacy, protocol compliance, patient education, eligibility screening, adverse event assessment, medication reconciliation, safety monitoring, documentation, regulatory reporting, and coordination among investigators, clinic nurses, research coordinators, and multidisciplinary teams.

Provides independent administrative coordination for Hematology Oncology faculty and clinical research programs. Responsibilities include calendar and travel management, reimbursements, personnel administration, faculty CVs and bibliographies, billing and statistical reports, manuscripts, space and equipment coordination, grant preparation, policy implementation, and special projects. The role supports investigators, coordinates with internal and external stakeholders, and requires discretion, accuracy, judgment, and familiarity with research or clinical environments.

Manages clinical research operations across community oncology sites, overseeing study startup, activation, conduct, enrollment, staffing, compliance, and closeout. Leads and develops site-based research staff, integrates trial activities into clinical workflows, coordinates with central teams, providers, sponsors, and CROs, and monitors operational metrics, quality, resources, and regulatory adherence.

Conducts routine and for-cause monitoring of investigator-initiated oncology clinical trials. Ensures protocol, Good Clinical Practice, institutional, and regulatory compliance; documents findings, manages corrective actions, identifies risks, and supports data integrity and participant safety. Collaborates with investigators and study teams, contributes to SOPs and quality-improvement initiatives, and mentors staff through onboarding and co-monitoring.

Coordinates hematopoietic cell transplantation survivorship studies, including patient screening, informed consent, enrollment, visit scheduling, protocol implementation, sample handling, data collection, quality control, regulatory documentation, adverse-event reporting, and billing compliance. Supports Principal Investigators, clinical teams, patients, and study monitors while maintaining accurate records and ensuring adherence to IRB-approved protocols, Good Clinical Practice guidelines, and institutional policies. The role is partially onsite and remote.

Supports faculty and research personnel with sponsored research administration, grant submissions, budgets, financial reporting, time and effort reconciliation, purchasing, compliance, and daily program operations. Coordinates regulatory documentation, faculty administrative activities, reporting, and external collaboration agreements. Provides strategic guidance on funding applications, monitors project expenditures, prepares financial projections, and coaches lower-level staff while working collaboratively across departments.

Coordinates investigator-initiated and industry-sponsored clinical trials under supervision. Responsibilities include identifying and consenting eligible patients, coordinating enrollment and sample collection, scheduling procedures, placing collection orders, maintaining study files and tracking systems, entering sample data, and transporting samples to receiving laboratories. The role also requires applying human research protections and regulatory requirements.

Provides pre- and post-award administration for sponsored research, including grant submissions, budgeting, financial reconciliation, compliance, reporting, effort tracking, procurement, and award closeout. Partners with investigators and program leaders on forecasting, regulatory requirements, operational planning, HR coordination, and research administration. Supports complex portfolios involving multi-site projects and subawards while generating reports and resolving financial discrepancies.

Coordinates Phase I–III clinical trials and cancer control studies, including patient screening, enrollment, consent, visit scheduling, specimen collection, data entry, documentation, billing review, monitoring visits, and regulatory compliance. Collaborates with clinical, data coordination, finance, and study-monitoring teams. The role supports oncology research involving radiopharmaceuticals and requires travel between Fred Hutch and UW Medical Center campuses.

Supports clinical research faculty with grant and award administration, budget monitoring, financial projections, time and effort reporting, compliance activities, purchasing, and general program operations. Coordinates research submissions, progress reports, regulatory applications, faculty administrative materials, onboarding, and performance processes. Partners with faculty and internal departments, prepares financial reports, manages sponsored and non-sponsored funds, and coaches junior staff in a hybrid academic research environment.

Manages day-to-day oncology clinical trial operations, including patient screening, enrollment, informed consent, visit coordination, protocol compliance, sample handling, research documentation, data entry, billing review, and monitoring-visit support. Serves as a liaison among patients, providers, investigators, clinical teams, and study monitors while maintaining regulatory and study records in accordance with GCP, institutional policies, and applicable requirements.

Conduct computational dry-lab experiments supporting cancer and infectious disease research. Maintain laboratory records, compile and interpret experimental data, report findings, attend lab meetings, and present scientific results. The intern will work under the Principal Investigator and senior laboratory technician, collaborate with lab personnel, assist with lab and cluster organization, and complete additional duties as needed.

Build and configure clinical trial calendars and budgets in OnCore using research protocols and negotiated payment terms. Perform quality assurance, system testing, data cleanup, reporting, and workflow documentation. Support CTMS users through help desk assistance, written communication, webinars, and meetings. Collaborate with research, budget, project management, health system, vendor, and central office teams while managing priorities, compliance requirements, deadlines, and institutional processes.

Supports clinical research studies evaluating lifestyle, behavioral, and nutritional interventions for cancer survivors. Responsibilities include participant screening, consent, enrollment, recruitment, data collection and entry, specimen handling, scheduling, data quality review, REDCap and CTMS management, regulatory documentation, study supply tracking, and community outreach. Spanish and English proficiency are required, with occasional evening and weekend work.