Remote Jobs for Reseachers, Research Engineers, Research Scientists, & Research Analysts

Lead design, build, and deploy of large-scale data platforms for LLMs, RAG, and agentic AI systems. Hands-on coding, architecting fault-tolerant pipelines, establishing MLOps/DataOps best practices, mentoring engineers, and operationalizing research into production across Exabyte-scale distributed systems.

Lead ThreatLabz’s threat research engagement strategy within Marketing. Develop positioning, messaging, content, and launch programs that translate complex security research into compelling narratives for CISOs, practitioners, information-sharing organizations, media, and AI-driven discovery. Partner with research, product, sales, enablement, and demand generation teams; empower sales with research-driven tools; monitor market and competitive intelligence; and lead hybrid, cross-disciplinary teams.

Leads Deepgram’s end-to-end Text-to-Speech research program, owning research strategy, technical direction, model development, evaluation, and production deployment. Advances neural audio modeling, prosody, expressiveness, multilingual generation, voice consistency, controllability, and inference performance. Builds and develops research teams, manages technical leaders, prioritizes experiments and compute, evaluates model quality, and partners with engineering and product leadership to ship production-grade models.

Leads product research and development for emerging mobility insurance products. Designs manuscript coverage for autonomous vehicles, teleoperation, platform liability, and mixed fleets; drafts policy forms, prepares filings, assesses compliance, and analyzes competitor offerings. Coordinates cross-functional initiatives with underwriting, claims, legal, actuarial, pricing, and strategy teams to develop scalable coverage solutions, support new business, and expand the mobility product portfolio.

Serve as the primary clinical partner to biopharma accounts, translating oncology practice, real-world evidence, clinical trials, and AI-driven solutions into strategic guidance. Develop account strategies, analyze pipelines and trial data, advise on protocol design and cohort selection, synthesize conference updates, and communicate complex scientific solutions to executive clients. Requires oncology clinical expertise, preferably in gastrointestinal or breast cancers, plus biopharma and real-world data fluency.

Lead global pharmaceutical and biotechnology client accounts for Tempus diagnostics and CRO offerings. Develop account strategies, exceed revenue goals, build executive and R&D relationships, negotiate complex agreements, identify opportunities across client portfolios, coordinate cross-functional teams, and support precision medicine case studies. Requires deep life sciences sales experience, diagnostic and drug development knowledge, and approximately 30% domestic and international travel.

Supports Epic and third-party healthcare applications through workflow analysis, testing, training, personalization, deployment, documentation, troubleshooting, and performance optimization. Serves as a liaison between IT and healthcare operations, ensures compliance with HIPAA and MIPS requirements, supports application integration, and mentors junior analysts. The role is hybrid and requires occasional onsite work and minimal travel within the Baptist Health region.

Research intern supporting next-generation memory and system architecture development for AI and datacenter workloads. Responsibilities include characterizing AI training and inference workloads, building analytical and simulation performance models, evaluating memory and integration technologies, validating models against reference data, and producing performance, efficiency, and cost analyses. The intern will document findings, contribute to technical reports and invention disclosures, and help quantify architectural tradeoffs for future memory products.

Conduct red-team assessments of formally verified systems, evaluating proofs, specifications, threat models, and trusted computing bases. Build AI-driven vulnerability discovery, triage, and exploit-generation tooling; identify and demonstrate exploitable weaknesses in software and infrastructure. Produce rigorous security reports, publish methodologies, collaborate with domain experts and third parties, and deliver engagements on fixed schedules.

The role involves supporting research collaborations in oncology, engaging KOLs, managing study proposals, and contributing to medical writing and strategy development.

Join a research and advisory pipeline for an asset-management startup building an auditable reasoning engine. Advise on agentic AI, world models, interpretability, and systemic risk. Help shape research direction, identify failure modes and guardrails, and provide scholarly evidence (papers, GitHub, Google Scholar) and a short written response to demonstrate expertise.

Research fellows will validate AI-generated paper reproductions, simulations, and results; map research areas; define standards for high-quality AI research; create benchmark tasks and evaluations; and contribute as lead or first authors to a public benchmark paper and evaluation release.

Conduct industry-focused AI research on autonomous agents and world models. Develop models involving large language models, active inference, and optimal policies, including architecture experimentation, fine-tuning, deep-learning agent development, and action optimization. Candidates will work on real-world enterprise problems while pursuing cutting-edge research during a fixed-term three- or six-month fellowship.

Own Deepgram’s end-to-end text-to-speech research program, including technical strategy, model architectures, experiments, training, evaluation, and production deployment. Lead researchers and technical managers, establish roadmaps, advance naturalness, expressiveness, multilingual generation, controllability, voice consistency, and inference efficiency, and partner with engineering and product leadership to ship high-quality models.

Support JMI's marketing team by creating customer profiles, helping develop targeting strategies for other interns, and completing a flexible, course-aligned market research project under mentor guidance.

Drive business development and revenue growth by identifying and qualifying leads, managing the sales pipeline, conducting demonstrations, negotiating contracts, forecasting, and closing opportunities. Build relationships with clinical research sites, sponsors, CROs, and academic institutions. Use CRM tools to track sales activity, collaborate with internal teams, stay informed on market trends, and execute sales strategies to meet targets.

Oversees clinical monitoring activities and CRA performance to ensure compliance with ICH-GCP, regulations, and company SOPs. Manages CRA resource allocation, quality indicators, site relationships, audits, inspections, risk resolution, and milestone delivery. Leads recruitment, onboarding, task assignment, performance evaluations, mentoring, and professional development for the CRA team. Supports monitoring competency assessments and cross-functional collaboration across clinical trials.

Supports clinical studies and investigational medical device programs for organ perfusion technology. Responsibilities include device and procedure training, clinical site support, protocol and study material development, data collection and review, database implementation, clinical study reports, FDA submission support, compliance monitoring, and technical feedback to engineering and development teams. Regular travel to research sites and case support are required.

Conduct independent research on frontier AI evaluation and auditing. Design rigorous evaluations, audit methods, and reproducible experimental pipelines; analyze model capabilities, risks, robustness, and alignment-relevant behavior. Produce audit reports, recommendations, publications, tools, and presentations while collaborating with technical, policy, engineering, and standards teams. The role requires careful handling of confidential information and may involve pilot audits with frontier AI companies.

Leads Cisco’s applied AI research organization, setting long-term research strategy across networking, security, programming, and human-computer interaction. Directs research teams, advances representation learning, structured prediction, generative models, and large language models, and translates prototypes into production enterprise solutions. Partners with product, engineering, and design teams, mentors researchers, and establishes ethical AI, privacy, security, and governance standards. Represents Cisco through publications, conferences, and external partnerships.

Conduct clinical trial site monitoring and management, including routine, initiation, and close-out visits; verify informed consent, protocol compliance, patient safety, and data integrity; manage CRF review, queries, registries, and serious adverse event reporting; coordinate with vendors and study teams; support employee training and local project coordination. The role requires two years of clinical monitoring experience, a relevant degree or allied health certification, and 60% overnight travel.

Conducts oncology clinical trial monitoring for assigned investigative sites, including site qualification, startup, initiation, monitoring, closeout, source document verification, query resolution, investigational product accountability, SAE reporting, regulatory compliance, and clinical data review. Communicates site status, resolves trial issues, maintains tracking systems and essential documents, and provides leadership or subject-matter expertise on complex studies and monitoring activities.

Leads full-cycle recruiting by developing sourcing strategies, screening candidates, managing candidate and hiring-manager communication, coordinating interviews, maintaining applicant tracking system data, analyzing recruiting metrics, and advising hiring managers on talent strategies and future hiring needs.

Lead and execute mixed-method healthcare research: design and program surveys, analyze quantitative and qualitative data, synthesize insights into executive reports and presentations, and deliver actionable recommendations to pharmaceutical and medtech clients.

Conduct clinical site qualification, initiation, monitoring, and termination visits; maintain site relationships; protect participant safety; support recruitment; ensure protocol, SOP, GCP, and regulatory compliance; assess data quality, site performance, drug accountability, and regulatory documentation. The role independently manages clinical monitoring activities across multiple therapeutic areas within a decentralized UK team.