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The Research Analyst Engineer is responsible for researching, gathering, and entering technical hardware and software specifications into internal databases. They also perform fact-checking, content editing, and ensure all web publications meet quality and tone guidelines.
The consultant will provide technical support for education sector planning, research, and monitoring activities under the GPE System Capacity Grant. Responsibilities include leading the development of education situation reports, managing data dashboards, and facilitating capacity-building initiatives for education stakeholders.
The Clinical Research Monitor ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and company procedures. They also manage relationships with investigators and site staff to support study initiation, patient recruitment, and data reporting.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will perform data review and collaborate with site staff to maintain high-quality clinical data and study documentation.
The Clinical Research Associate will coordinate clinical trial monitoring activities, maintain study documentation, and ensure compliance with protocols and regulatory requirements. They will also manage stakeholder relationships and oversee study cost efficiency to ensure high-quality clinical outcomes.
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The Research Analyst Engineer will conduct internet research and data analysis to maintain accurate product specifications for hardware and software in internal databases. They are responsible for fact-checking, editing, and writing high-quality product descriptions to ensure compliance and visibility on e-commerce platforms.
The Associate Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols within a country. This role acts as the main point of contact between Country Operations and the clinical trial team to ensure compliance with ICH/GCP regulations and internal quality standards.
The Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols in compliance with regulatory standards. They act as the main point of contact between Country Operations and clinical trial teams, leading local study teams to ensure high performance and adherence to timelines.
The Senior Research Associate leads scientific coordination, project management, and the design of de novo data collection projects. They are responsible for drafting scientific deliverables, engaging with project stakeholders, and contributing to business development activities.
Design, implement, and evaluate model-based reinforcement learning agents and planning-based controllers for industrial control systems. Develop learned dynamics and world models while mentoring research engineers to translate research into practical production outcomes.
Design and implement machine learning and optimization algorithms to improve ad quality and performance within the ad marketplace. Partner with product teams to define optimization objectives and communicate technical results to stakeholders.
Manage the full lifecycle of grant activities from proposal submission through closeout for assigned departments. Provide expert guidance to faculty and staff regarding sponsor guidelines, compliance regulations, and institutional policies.
The researcher will support the development of innovative approaches to address challenges in modern power system dynamics and grid security. They will collaborate with diverse teams to execute research tasks and contribute to high-quality technical publications and proposals.
The Clinical Research Manager Lead is responsible for the end-to-end performance of clinical trials within specific therapeutic areas, ensuring adherence to regulations and company standards. They provide line management to CRM teams, oversee study execution, and collaborate with cross-functional stakeholders to drive country-level clinical research capabilities.
The role involves leading research and engineering for the full lifecycle of large language models, including data curation, pretraining, and fine-tuning. You will collaborate with cross-functional teams to build scalable training pipelines and deliver high-impact AI solutions for enterprise customers.
The intern will support the research team by conducting quantitative and qualitative research, performing literature reviews, and analyzing postsecondary education data. Additionally, they will assist in preparing research reports, presentations, and logistics for organizational convenings.
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The role involves conducting laboratory, field, or computational research activities and managing research data. Responsibilities also include maintaining equipment, contributing to manuscripts, and collaborating with faculty and research personnel.
You will review initiation of coverage draft notes and accompanying financial models to evaluate the accuracy of valuation methodologies. Additionally, you will identify analytical gaps, accounting inconsistencies, and provide structural feedback on the research reports.
The research scientist will lead research work across the lab, co-develop lab strategy, and coordinate systems for activities across various workstreams. Responsibilities include designing measurement instruments, coordinating multi-site data collection, and developing grant proposals and manuscripts.
The Director of Research and Development will oversee the technical strategy, cloud infrastructure, and migration of the Total Service Cloud ERP platform. They will lead the engineering team, manage AI-assisted development pipelines, and ensure the correctness and reliability of financial and operational modules.
The Associate Director will develop and implement patient-centric recruitment and engagement strategies to optimize clinical trial performance. They will serve as a strategic advisor to clients, translating complex study needs into actionable, innovative operational plans.
The Associate Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols within a country. This role acts as the main point of contact between Country Operations and clinical trial teams, ensuring compliance with ICH/GCP regulations and internal quality standards.
The Clinical Research Manager is responsible for the end-to-end project management and performance of assigned clinical protocols in compliance with regulatory standards. They serve as the primary point of contact for clinical trial teams, ensuring successful site selection, recruitment, and execution while leading local study teams.
The Clinical Research Manager Lead is responsible for the end-to-end performance of clinical trials within specific therapeutic areas, ensuring adherence to local regulations and company SOPs. They provide line management to CRM staff, oversee study metrics, and collaborate with cross-functional stakeholders to drive site and investigator development.
The Research Administrative Coordinator provides high-level operational support to the VP of Research and the OneR leadership team. Responsibilities include managing calendars, coordinating meetings, preparing performance reports, and overseeing contractor documentation.
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The adjunct faculty will instruct students in technical and quantitative competencies, including GIS, statistical analysis, and research design for crime and intelligence analysis. They are also responsible for evaluating student performance in AI-supported analytic outputs and integrating ethical stewardship into the curriculum.
The research scientist will lead research work across the lab, co-develop lab strategy, and coordinate systems for activities across various workstreams. Responsibilities include designing measurement instruments, coordinating multi-site data collection, and developing grant proposals and manuscripts.
Research assistants will support Darden faculty by locating and summarizing academic literature and policies. They will also construct data sets, perform qualitative coding, and summarize research for business practitioners.
The associate will support research communities in sharing biomedical data by managing access requests and ensuring compliance with ethical and regulatory standards. They will also assist in operational tasks such as tracking data sharing agreements and documenting internal processes.
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