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

Develop geometry-processing and simulation algorithms for engineering applications, build services for 2D/3D CAD, CAE, and CAM data, create rendering modules, curate datasets, optimize machine learning post-training workflows, and contribute to engineering domain-specific languages. The role requires strong Python development, computational design or geometry-processing experience, machine learning expertise, and familiarity with CAD/CAM/CAE tools, LLM post-training, and compilers or DSLs.

Supports clinical trial execution for AbbVie’s neurology programs under supervision. Serves as a primary site contact, trains and engages investigators and staff, conducts site monitoring, evaluates recruitment and data quality, assesses risks, supports corrective actions, and maintains compliance with protocols, GCP, ICH guidelines, regulations, and company procedures. The role also supports investigator and site selection, safety reporting, inspection readiness, and payment administration.

Manages clinical trial sites throughout study phases, ensuring ICH/GCP, regulatory, protocol, data quality, and patient-safety compliance. Performs site selection, validation, initiation, monitoring, and close-out visits; maintains regulatory documentation and clinical systems; resolves performance and compliance issues; supports audits and inspections; develops site relationships and recruitment capabilities; and contributes clinical monitoring expertise across internal and external teams. Requires approximately 65%–75% domestic and international travel.

Manages clinical trial sites and protocols for immunology studies, ensuring ICH/GCP, regulatory, safety, quality, and documentation compliance. Serves as the primary site contact, conducts remote and on-site monitoring visits, supports site selection and activation, manages performance and recruitment issues, maintains CTMS/eTMF records, and contributes to audits, inspections, process improvements, and site development. Requires 65–75% domestic and international travel.

Designs, administers, automates, and enhances Azure Virtual Desktop environments in a classified government setting. Responsibilities include managing host pools and session hosts, creating Windows and Linux images, deploying applications, monitoring performance, troubleshooting complex infrastructure issues, applying security hardening, executing upgrades and patching, and supporting incident response, root-cause analysis, and capacity planning.

Conduct vulnerability scanning, triage, remediation validation, threat hunting, and security monitoring across Azure infrastructure and containerized workloads. Maintain secure baselines, integrate security controls into CI/CD pipelines, analyze Microsoft Sentinel alerts, and prepare vulnerability reports, dashboards, POA&M updates, and compliance artifacts. Collaborate with engineering and compliance teams to align cloud security with DoD RMF, NIST, CMMC, and FedRAMP-equivalent requirements.

Support cybersecurity governance, compliance, and security hardening for a DoD DevSecOps Azure cloud environment. Manage RMF, A&A, ATO, eMASS artifacts, CMMC, NIST, FedRAMP, and continuous monitoring requirements. Conduct risk assessments, vulnerability testing, audits, remediation, and threat-informed security activities. Collaborate with authorizing officials, government stakeholders, auditors, and engineering teams while developing policies, delivering briefings and training, and guiding secure technical decisions.

Develop applied AI research prototypes and systems for agentic marketing applications, focusing on generative image and video, brand asset creation, data workflows, and autonomous evaluation. The role combines probabilistic and quantitative reasoning, backend system architecture, product intuition, experimentation, and customer-focused product development. Responsibilities include building proofs of concept, improving AI-generated media realism and brand alignment, and architecting agentic systems.

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 and resolve data queries; and contribute to protocols and clinical study reports. The role requires extensive travel, independent monitoring experience, strong clinical research knowledge, and familiarity with ICH-GCP guidelines.

Manages global neuroscience clinical research projects for biotech, medtech, and pharmaceutical clients. Coordinates cross-functional teams, budgets, scopes, timelines, regulatory activities, and project delivery. Serves as the primary client liaison, leads project meetings, supports proposals and business development, and develops client relationships to generate future business.

Supports clinical trial execution in neurology by partnering with investigative sites, training site staff, conducting monitoring activities, ensuring protocol and regulatory compliance, assessing risks, supporting patient recruitment and retention, maintaining data quality, and preparing sites for audits and inspections. Works under supervision while developing therapeutic-area, clinical research, and site-management expertise.

Develop deep learning and AI/ML models to predict cardiac events from ECG and physiological signals. Apply signal processing, analyze implantable-device datasets, build Python tools, validate algorithms, and support feasibility studies for diagnostic features. Collaborate with clinical, software, and hardware teams to improve implantable-device performance and patient outcomes.

Supports the vice chair with research, analytical work, and special projects. Responsibilities include copy editing, proofreading, reference management, locating journal article PDFs, formatting and submitting manuscripts, preparing digital images for publication, and supporting posters, presentations, reports, and correspondence.

Supports seasonal agricultural research operations, including planning, planting, phenotyping, pollinating, data collection, packaging, and harvesting yield trials. Operates and maintains agricultural machinery and research equipment, ensures trial data accuracy, supervises employees and contract labor, resolves minor issues, and communicates project status. The role requires agronomic knowledge, precision agriculture experience, safety compliance, and proficiency with data collection and reporting systems.

Advise law firms and research departments on AI adoption, workflow design, responsible use, vendor products, training, and post-launch support. Lead client discovery, testing, presentations, workshops, and implementation programs. Build relationships with legal technology vendors, translate product updates into practical guidance, and develop internal AI capabilities, reusable methods, and thought leadership.

Manages oncology clinical trial sites through qualification, initiation, monitoring, activation, and close-out. Ensures data integrity, subject safety, inspection readiness, regulatory compliance, and adherence to protocols, GCP, SOPs, and applicable regulations. Reviews risk indicators, resolves issues, develops CAPA plans, supports IRB and regulatory submissions, trains site staff, and maintains site relationships. Requires solid tumor oncology monitoring experience and up to 50% travel.

Own and grow strategic pharmaceutical and biopharmaceutical manufacturing accounts through consultative selling and executive-level relationship management. Develop account plans, identify growth opportunities, analyze sales data, lead cross-functional execution, negotiate commercial agreements, and achieve revenue objectives. The role requires extensive regional travel across the Research Triangle area, with customer visits at least four days per week.

Supports clinical trial execution at investigative sites under supervision. Responsibilities include site evaluation, training, monitoring, risk assessment, corrective action planning, data quality oversight, safety-event follow-up, recruitment support, regulatory compliance, inspection readiness, and investigator payment administration. Builds relationships with investigators and site staff while ensuring adherence to protocols, Good Clinical Practice, ICH Guidelines, regulations, and company procedures.

Leads prospective and retrospective reviews of clinical trial protocols, billing grids, charge segregation, Medicare Coverage Analysis, and EPIC billing transactions. Audits compliance with CMS research-billing regulations, analyzes financial and operational data in Excel, identifies corrective actions, and presents findings to executive leadership. Supports legal, compliance, research administration, and revenue-cycle initiatives while improving regulatory oversight processes, controls, workflows, and reporting tools.

Leads clinical evidence generation and dissemination strategies for new product development and lifecycle management projects in orthopaedics. Develops protocols, study materials, budgets, reports, clinical evaluation reports, and regulatory submission content. Partners with Clinical Operations, Biostatistics, Regulatory Affairs, Medical Affairs, and investigators to deliver compliant clinical programs on time and within budget. Supports regulatory discussions, evidence interpretation, trial registration, and market access activities.

Conduct intelligence analysis and technology assessments focused on remote sensing, electronic warfare, radar, and emerging military technologies. Identify and prioritize promising technologies, evaluate foreign research using open and classified sources, synthesize findings into reports, and identify relevant conferences and research actors. Collaborate with government, military, contractor, and technical personnel on science, technology, and innovation problems.

Conducts clinical trial site monitoring and management, including site initiation and close-out visits, protocol compliance, informed consent verification, source data review, CRF review, query resolution, SAE reporting, registry management, vendor coordination, and staff training. The role requires clinical monitoring experience, ophthalmology or oncology expertise, frequent overnight travel, strong adaptability, and proficiency with electronic clinical data systems.

Manages multiple quantitative market research projects from inception through delivery. Responsibilities include questionnaire development, fieldwork management, data processing and multivariate analysis oversight, data synthesis, report creation, quality-checking toplines and reports, and mentoring Junior Project Directors. The role translates research findings into actionable business insights for clients and operates fully remotely within Eastern Time Zone business hours.

Manages full-cycle recruiting for research and development roles, including sourcing, screening, interviewing, candidate presentation, client consultation, negotiation, and closing. Builds candidate networks through market research and passive sourcing, maintains client and candidate relationships, tracks recruiting metrics, manages pipeline activity, and achieves submit and hiring goals. Requires strong recruiting expertise, communication, prioritization, computer, applicant tracking system, and client relationship skills.

Leads the full equity research publishing lifecycle, including editorial review, supervisory approval, production, quality control, regulatory compliance, and distribution. Oversees publishing systems and high-volume workflows while ensuring adherence to FINRA requirements, internal controls, and risk standards. Builds and develops a high-performing research publishing team, partners with stakeholders, and drives accuracy, timeliness, professional presentation, and continuous improvement.