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The Associate Director provides consultative support and expert advice to higher education leaders to help them achieve strategic goals. They deliver high-impact presentations, facilitate workshops, and build relationships with senior executives to drive institutional transformation.
The Director provides consultative support and expert advice to higher education and K-12 leaders to help them navigate strategic, financial, and mission-consequential challenges. They are responsible for delivering high-impact presentations, facilitating workshops, and generating original research insights to support client success and business development.
The role involves designing and evaluating applied AI solutions across various domains while bridging the gap between research and production engineering. You will be responsible for building scalable ML pipelines, optimizing model performance, and ensuring alignment with business needs and safety standards.
The librarian will research and draft a development plan for a new library to support the Ted Stevens Center for Arctic Security Studies. They will produce a report outlining best practices for virtual and physical material access, cataloging, and storage.
The Research Assistant will perform laboratory tasks, including epigenetics and molecular biology techniques, to support research on age-related macular degeneration and ocular cancers. They will also assist in data collection, scientific writing, and the maintenance of laboratory equipment and cell lines.
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The Clinical Research Associate I supports the research team by performing study startup, implementation, and closeout activities. They are also responsible for managing regulatory submissions, maintaining compliance, and interacting with patients for data collection and informed consent.
The Senior Research Director leads a pod of researchers to deliver exceptional client outcomes while managing high-impact research engagements. They are responsible for team development, operational optimization, and driving business growth through customer retention and upsells.
The intern will complete a quantitative research project to assist the Football Information department in identifying key insights. The role involves working independently on a single research project over a 10-week period.
You will design and build scalable data pipelines for multimodal agent training, including collection, curation, and quality assurance. You will also collaborate with research scientists to develop evaluation datasets and maintain infrastructure for efficient data loading and storage.
The research fellow will collect, organize, and analyze data to support IDRA's research and evaluation team. They will also participate in strategy discussions, contribute to advocacy work, and conduct site visits at various educational institutions.
The Senior Clinical Research Associate will conduct remote and onsite monitoring visits to ensure data integrity and patient safety in accordance with clinical study plans. They are responsible for maintaining Trial Master Files and ensuring all site documentation is accurate and compliant with ICH/GCP guidelines.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure data integrity, patient safety, and adherence to regulatory standards. They will manage site activities, maintain Trial Master File documentation, and conduct qualification, initiation, and close-out visits.
The Junior Researcher will manage and analyze quantitative and qualitative datasets to support education research projects within the Airbel Impact Lab. They will also contribute to the dissemination of findings by drafting reports, briefs, and blog posts for diverse audiences.
The Project Director oversees a portfolio of clinical studies and manages the Project Managers responsible for their execution. They are also responsible for business development activities, client satisfaction, and ensuring all studies adhere to regulatory and quality standards.
The Project Director oversees a portfolio of clinical studies and manages project managers to ensure operational excellence and client satisfaction. They are responsible for financial oversight, risk mitigation, and driving business development activities while maintaining compliance with regulatory standards.
Participants will engage in various research activities such as completing online questionnaires, participating in remote discussions, and testing new concepts. These activities are designed to gather opinions on products and services for research purposes.
The Director will lead clinical matrix teams and oversee the development of clinical study protocols and scientific documentation for regulatory submissions. They are responsible for monitoring clinical safety and efficacy data while collaborating with cross-functional teams and external experts.
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The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct risk-based monitoring, manage documentation, and facilitate communication between investigative sites and sponsors.
The analyst supports the implementation, maintenance, and evaluation of research applications while providing technical support and issue resolution. They also collaborate with cross-functional teams to optimize workflows, manage system configurations, and develop custom reports.
You will conduct clinical trial monitoring activities, including site visits and ensuring protocol compliance and data integrity. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and maintain high-quality clinical data.
The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with investigators and site staff while performing data review to maintain high-quality clinical data.
The Research Coordinator manages the administrative, logistical, and workflow components of interdisciplinary social science and education research projects. This role facilitates team communication, ensures research compliance, tracks project milestones, and supports financial and grant administration.
The Clinical Research Manager is responsible for the end-to-end performance and project management of assigned clinical protocols in compliance with ICH-GCP and company standards. They serve as the primary point of contact for clinical trial teams, overseeing site selection, recruitment, and risk management while ensuring high-quality execution.
The role involves testing, evaluating, and improving AI systems by performing tasks such as data annotation, content review, and prompt creation. You will also conduct research, analyze digital content, and test software or workflows based on project requirements.
The Research Executive is responsible for the operational implementation and coordination of market research projects, including survey programming and fieldwork monitoring. They will collaborate with Research Consultants to ensure high-quality data delivery and support the generation of impactful client insights.
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You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits. Additionally, you will ensure protocol compliance, maintain data integrity, and collaborate with investigators to facilitate smooth study conduct.
The intern will support the business development team by researching funding opportunities, designing sustainable finance proposals, and managing bid pipelines. They will also produce analytical research memoranda and create presentations to assist senior leaders in client engagement.
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