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

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%).

Monitor clinical trials through site qualification, initiation, monitoring, and close-out. Ensure protocol compliance, data integrity, and patient safety. Perform data review and query resolution, collaborate with investigators and site staff, and contribute to study documentation and reports.

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, and contribute to study documentation including protocols and clinical study reports.

Coordinate and perform clinical trial monitoring activities, maintain study documentation, handle sponsor queries, support study setup and feasibility, ensure protocol and regulatory compliance, and build relationships with investigators and site staff. Travel (~60%) required.

Serve as primary site contact for neuroscience clinical trials, conducting site selection, training, routine and closure monitoring, ensuring GCP/ICH compliance, data quality, patient safety, risk assessment and corrective actions, mentoring junior CRAs, and supporting investigator relationships to drive recruitment and study performance.

Partner with investigative sites to support clinical trial conduct and data integrity. Conduct site evaluation, training, routine and closure monitoring under supervision. Monitor site performance and safety, implement risk mitigation and corrective actions, and support investigator/site selection. Ensure regulatory compliance (ICH/GCP), audit readiness, timely data and safety reporting, and manage investigator payments as applicable.

Provide clinical site monitoring and management for trials including initiation, routine and close-out visits; ensure regulatory compliance and informed consent; perform CRF review, SAE reporting and query resolution; coordinate local project activities and train/co-monitor staff. Frequent travel and use of electronic data capture required.

Monitor clinical trial sites including initiation, routine monitoring, and close-out. Ensure protocol adherence, informed consent, data integrity (CRFs/EDC), SAE reporting, registry management, feasibility, and coordinate local project activities. Provide training and liaise with vendors and clients; perform on-site and remote monitoring with significant travel.

Coordinate multiple clinical research projects for transplant PIs: collect and document patient data per protocol, perform patient assessments and phlebotomy, oversee source documentation and QA, train and mentor research staff, support enrollment and study initiation, assist with budgets and specimen handling, and ensure regulatory compliance.

Provide virtual counseling visits for clinical trial participants within licensure scope, schedule appointments, complete and submit source documentation, follow clinical research guidelines to support participant well-being and retention, and maintain required licenses and credentials.

Manage a portfolio of academic accounts to drive revenue for AI-powered research intelligence products. Use consultative selling to build relationships with libraries and research offices, develop account strategies, forecast pipeline in CRM tools, gather market insights, and represent Elsevier at conferences to generate pipeline and expand long-term partnerships.

Accountable for site performance and regulatory compliance for assigned immunology clinical trials. Acts as primary site contact, performs on-site and remote monitoring, manages regulatory documentation in CTMS/eTMF, supports site selection and start-up, escalates issues, conducts visits (initiation/monitoring/close-out), and contributes as SME to monitoring processes. Requires extensive travel and cross-functional collaboration to protect subject safety and data integrity.

Lead long-horizon R&D to define future decision intelligence: explore reasoning architectures, prototype and formalize system primitives, evaluate new signal classes, and translate research into reusable components aligned to strategic product direction.

Build and maintain experimental decision-system prototypes, evaluation tooling, simulation environments, and research infrastructure to enable rapid iteration and validation of research concepts in real-world constraints.

Apply formal decision theory and structured reasoning to enterprise problems: design decision frameworks, model uncertainty and tradeoffs, test decision architectures, run experiments, and translate research into system-ready primitives collaborating with engineering and product teams.

Lead end-to-end quantitative research projects for assigned clients: scope, design surveys, define samples, analyze data, and deliver client-ready insights and recommendations. Serve as primary client contact, guide clients to full-service or DIY solutions on Numerator's platform, use AI-enabled tools responsibly, mentor analysts, support sales and consulting efforts, and manage multiple projects while protecting scope, quality, and timelines. Travel as required.

Lead and execute strategic primary and secondary market research across US commercial businesses, managing complex projects, vendors, cross-functional teams, budgets, compliance, and delivering actionable insights to inform marketing and product decisions.