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

The Research Operations Specialist will oversee system card production, ensuring clear communication and consistency in safety documentation created by researchers, while managing project timelines and contributor coordination.

Monitor and manage clinical trial sites including qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; perform data review and query resolution; collaborate with investigators and site staff; contribute to study documentation and clinical study reports.

Lead clinical trial monitoring to ensure protocol and regulatory compliance, conduct site visits, resolve issues, mentor CRAs, collaborate with cross-functional teams, and maintain data integrity and site performance. Travel required (~60%).

Lead clinical trial monitoring activities to ensure protocol and regulatory compliance, conduct site visits, resolve issues, support data integrity, train site staff and CRAs, collaborate cross-functionally, and maintain strong site relationships to drive successful trial execution.

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; review data and resolve queries; contribute to study documentation and clinical study reports.

Lead site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensure protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff, perform data review and queries resolution, and contribute to study documentation and clinical study reports.

Lead and conduct clinical research projects, design trials per regulatory standards, analyze and interpret data, produce scientific reports, collaborate with cross-functional teams, ensure compliance, and publish findings.

Executive leader responsible for driving growth of Spire Outsourcing's financial planning business: strategy, business development, client relationships, team leadership, operations scalability, and industry representation. Ensures delivery of high-quality financial planning services and meets revenue targets.

Lead research and intelligence direction for a high-frequency AI assistant: set model and systems strategy (memory, reasoning, planning), choose architectures, define real-world evaluation and safety frameworks, drive frontier techniques, and partner with product and engineering to ship robust, production ML systems.

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.

The VP of Research, Machine Learning will set research direction for AI systems, focusing on context representation, reasoning, and evaluation frameworks while ensuring product safety and alignment.

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.

Lead coverage of how AI infrastructure is financed by analyzing lenders, structures, collateral, and credit risk. Build quantitative models, proprietary datasets, stress scenarios, and publish flagship research for investors, regulators, and industry stakeholders.

Support digital marketing and community efforts in MENA: gather and manage data for content and campaigns, handle community queries on Telegram/Discord, use campaign portals (Task On, Galaxy, Zealy), conduct data research, assist lead generation, monitor campaign metrics, and follow the content plan to improve engagement and ROI.

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.

Work directly with founders to research AI SaaS markets, identify high-fit accounts and buyers, prepare personalized outbound, maintain CRM discipline, track replies/objections, run GTM experiments, and support founder-led sales to create real customer conversations.

Monitor and manage clinical trial activities including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and site staff; and contribute to study documentation and clinical study reports. Approximately 60% travel required.

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data review and query resolution; and contribute to study documentation including protocols and clinical study reports.

Monitor and support clinical trial sites through qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, and patient safety; resolve data queries; collaborate with investigators and prepare study documentation including protocols and clinical study reports.

Monitor and manage clinical trial activities including site qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, patient safety, resolve queries, and contribute to study documentation and reporting.

Monitor and manage clinical trial site activities including qualification, initiation, monitoring, and close-out visits. Ensure protocol compliance, data integrity, patient safety, query resolution, and contribute to study documentation and reporting. Collaborate with investigators and site staff to support high-quality trial conduct.

Monitor clinical trials (site qualification, initiation, monitoring, close-out), ensure protocol compliance, data integrity, and patient safety. Review and resolve data queries, collaborate with investigators and site staff, and contribute to study documentation and clinical study reports. Approximately 60% travel; requires CRA monitoring experience and ICH-GCP knowledge.

Manage clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with site staff and investigators; perform data review and query resolution; contribute to study documentation and reports.

Perform clinical trial monitoring and study setup activities, maintain study documentation and status reports, manage sponsor queries, support study feasibility and documentation, build relationships with investigators and site staff, and ensure compliance with protocols, ICH-GCP, and regulatory requirements to protect patient safety.

Conduct and coordinate clinical trial monitoring activities, maintain study documentation, manage sponsor queries, support study setup and feasibility, ensure regulatory and protocol compliance, and build collaborative relationships with investigators and site staff. Role requires frequent travel (~60%).