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The Senior Research Specialist leads complex research and evaluation initiatives to advance student success and equity within the California Community Colleges system. This role involves managing the full project lifecycle, analyzing large datasets, and translating findings into actionable policy recommendations.
Participants will engage in various research activities such as completing online questionnaires, participating in remote discussions, and testing concepts. They will provide feedback on products and services to assist in research studies.
The analyst will interpret clinical trial agreements and budgets to configure them accurately within the CRIO system. They will also serve as a liaison between finance, clinical operations, and accounts receivable teams to ensure timely revenue recognition and sponsor invoicing.
The Specialist will contribute to advancing student success and equity by developing policy briefs, reports, and research projects. They will also manage project deliverables and foster strong relationships with diverse stakeholders across the California Community Colleges system.
Independently provide site management and monitoring support for clinical studies to ensure compliance with protocols, GCP, and regulatory standards. Collaborate with cross-functional teams and investigational sites to manage study deliverables, data integrity, and site activation activities.
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You will lead the development of simulation-based cost-effectiveness models in R and Excel for global pharmaceutical and biotech clients. Additionally, you will collaborate with a specialized team to interpret clinical study results and contribute to technical reports and client-ready deliverables.
You will lead the Threat Research Team, setting the research agenda and detection content roadmap while managing both adversary research and detection engineering. You are responsible for building capabilities against AI-related threats and ensuring the quality of detection content shipped to customers and the Falco community.
Participants will engage in various research activities such as completing online questionnaires, participating in interviews, and joining focus groups. You will provide feedback on products and services to help identify relevant research studies.
The Senior Research Analyst will contribute to the development and implementation of research and evaluation plans for K-20 education and substance use prevention programs. Responsibilities include analyzing qualitative and quantitative data, developing SAS code, and preparing technical reports for various stakeholders.
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 coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data reliability through rigorous review and problem-solving.
You will collaborate with a specialized team to build and program health economic simulation models in R and Excel for global pharma and biotech clients. Additionally, you will contribute to the development of study deliverables, including model conceptualization, analysis plans, and technical reports.
The Project Manager acts as the primary point of contact for clients, managing the full lifecycle of market research projects from initiation to final delivery. They are responsible for coordinating internal and external teams to ensure projects are completed on schedule, within budget, and meet high-quality standards.
The analyst is responsible for preparing and maintaining clinical trial budgets, including comparative reviews and setting up payment milestones. They also manage cost analysis, interpret protocols, and ensure billing compliance while collaborating with internal finance and research teams.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure protocol adherence and data integrity. They also provide guidance to site staff, manage site documentation, and verify source documents for patient safety and compliance.
The Clinical Research Associate is responsible for site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity. They also provide mentorship to site staff and ensure all site-related documentation is accurately filed in the Trial Master File.
Design and implement mathematical optimization models to solve complex industrial problems such as planning, scheduling, and resource allocation. Collaborate with cross-functional teams to integrate optimization workflows with AI solutions and build scalable production pipelines.
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The intern will design and execute evaluation projects to measure the impact and behavioral changes of program participants. They will also develop data collection instruments, analyze program data, and create reports for stakeholders.
Prospect and build new business within an assigned territory of education institutions while managing the full sales cycle. Conduct live presentations and diagnostic evaluations to map EAB's research and advisory solutions to the strategic needs of senior executives.
The Project Manager will own the end-to-end lifecycle of UX Research vendor engagements, including intake, contract execution, and invoicing. They are responsible for managing a high-volume portfolio, identifying blockers, and driving process improvements to ensure efficient research operations.
![Nevada System of Higher Education is hiring for remote Research Administrator, Pre Award with the Office of Sponsored Programs (REMOTE) [R0153457]](/assets/70cd76b6-14dd-4fa5-a096-89a3f4e325a8.jpg){kind=small}
The Research Administrator assists faculty and staff with the development, preparation, and submission of complex sponsored research proposals. They are responsible for ensuring compliance with university policies and federal regulations while managing proposal budgets and grant management systems.
Interns will assist with qualitative research activities, including data collection, coding, and analysis to support the development of peer-reviewed manuscripts. They will also conduct literature reviews and collaborate with research team members to contribute to project dissemination efforts.
The Clinical Research Associate II manages clinical study sites to ensure data quality, regulatory compliance, and audit readiness. They also facilitate site initiation, monitor protocol adherence, and manage device accountability and study documentation.
The Senior CRA will perform quality and compliant investigator site monitoring and management to ensure subject safety and data integrity. They will collaborate with cross-functional teams and external vendors to oversee study activities from start-up through close-out.
The Senior CRA will perform quality and compliant investigator site monitoring and management to ensure subject safety and data integrity. They will collaborate with cross-functional teams and external vendors to oversee study milestones from start-up through close-out.
The Operations Intern will support daily organizational functions including scheduling, data management, and event planning while contributing to special projects. They will also identify opportunities to improve internal systems, workflows, and organizational databases to enhance operational effectiveness.
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The Senior CRA will manage 2–3 clinical trials, overseeing site management activities including study start-up, monitoring, and closeout. They are responsible for ensuring data quality, regulatory compliance, and providing support to site staff throughout the clinical research process.
The scientist will lead R&D projects from concept through commercialization, including pilot runs and production start-ups. They will also collaborate cross-functionally to solve technical manufacturing challenges and advance innovation opportunities.
The Director will establish and lead the HEOR capability within Medical Affairs, developing integrated value-evidence strategies to support clinical development and launch readiness. They will partner cross-functionally to generate real-world evidence and economic models that address the needs of payers, HTA bodies, and healthcare systems.
The Senior CRA is responsible for the management and oversight of clinical study sites to ensure data quality and patient safety in accordance with regulatory guidelines. They perform site monitoring visits, manage recruitment strategies, and ensure compliance with study protocols and documentation requirements.
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