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The Research Engineer will translate complex research hypotheses into tangible AI applications and build robust infrastructure for scientific experimentation. They will also lead scientific publications and collaborate across multidisciplinary teams to integrate theoretical research into practical business solutions.
The Market Research Associate is responsible for recruiting respondents for healthcare market research projects and managing panel engagement in the Scandinavian region. They will perform cold calling, schedule interviews, and troubleshoot inquiries to ensure project delivery within specified timelines.
The Market Research Associate is responsible for recruiting respondents for healthcare market research projects and managing panel building initiatives in the Scandinavian region. They will also provide high-quality support to panel members, resolve inquiries, and ensure data quality through verification and troubleshooting processes.
Design and maintain large-scale web crawlers and high-throughput data collection systems for research and model development. Develop pipelines for data cleaning, normalization, and quality monitoring while collaborating with research teams to meet modeling needs.
The Clinical Research Associate II is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with site staff and investigators to facilitate study conduct and prepare essential study documentation.
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The intern will conduct research on emerging cybersecurity threats, vulnerabilities, and trends while analyzing data to support incident response. They will also collaborate with the team to develop innovative threat intelligence solutions and stay updated on industry best practices.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while overseeing observational and non-interventional studies.
The research assistant will deliver remote behavioral intervention sessions via Zoom and manage participant recruitment and data collection. They will also support daily research operations, including data entry, IRB compliance, and team coordination.
Conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Collaborate with site staff and investigators while performing data review to maintain high-quality clinical documentation.
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
The Doctoral Research Chair will guide doctoral candidates through their research process, ensuring methodological soundness and compliance with university policies. They are responsible for providing detailed feedback on qualitative and quantitative research while supporting the academic and spiritual development of students.
As a Senior Consultant, you will conduct comparative research and evaluation projects on gender equality and non-discrimination. You will also manage project teams, support methodological aspects, and ensure high-quality delivery of project work.
The specialist will oversee the screening, assessment, and retention of participants in a Randomized Controlled Trial (RCT) involving Deaf adults with mental health disorders, conducting all study activities remotely via Zoom. Key duties include performing mental health and suicide risk assessments in ASL, coordinating follow-up assessments, assisting with data management, and ensuring participant safety according to protocol.
The Principal Product Manager will own product roadmaps for AI-powered tools, manage backlogs, and define requirements for agentic AI systems that automate complex workflows. They will also identify opportunities for agentic AI transformation internally and research emerging AI technologies for product integration.
The Senior Recruiter will own recruiting for Researcher, Program Officer, Senior Researcher, and Senior Program Officer roles, working closely with research team leaders to improve assessment effectiveness and identify new candidate sourcing channels. This involves hands-on sourcing, screening, closing offers, and using data to drive evidence-based decisions about the hiring process.
The Clinical Research Associate is responsible for maintaining data integrity and quality, ensuring site compliance with ICH GCP and local requirements, and acting as the primary contact for assigned clinical sites from initiation through close-out. Key duties involve performing monitoring visits (virtual and on-site), resolving site issues, assessing site performance, and managing study documentation and systems.
The Research Analyst will collaborate with portfolio managers to define research goals, lead studies, and interpret data to recommend new investment ideas suitable for clients and institutional portfolios. Responsibilities include developing deep industry knowledge, gathering research data, maintaining databases, and building financial models for forecasting and analysis.
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The engineer will partner with research scientists to prototype and validate novel modeling ideas, scaling them through robust training systems for speech technologies, internal tooling, and innovative data strategies. Key duties involve architecting scalable training systems for STT/TTS models, designing internal UIs for ML workflows, and overseeing training tooling, job orchestration, and data storage.
The role involves working on research and development projects in applied cybersecurity, including concept development and project management tasks. Responsibilities also include preparing project reports, scientific publications, and presenting research findings at conferences.
This role is responsible for all aspects related to assigned clinical trial monitoring and site management, ensuring compliance with protocol, regulatory, and ICH GCP obligations across site initiation, routine monitoring, and close-out activities. Key duties include performing on-site and remote monitoring, verifying source document accuracy, writing and submitting reports, and escalating observed deficiencies.
The role involves executing project recruitment tasks across Scandinavia and other assigned markets by contacting panelists via phone and cold calling to schedule interviews. Key duties also include proactive panel building, managing panelist inquiries, investigating fraud, and ensuring recruitment targets are met within specified timelines.
The role involves executing project recruitment tasks across Scandinavia and other assigned markets by contacting panelists via phone and cold calling to schedule interviews. Responsibilities also include proactive panel building, managing member inquiries, investigating fraud, and ensuring recruitment targets are met within specified timelines.
The Senior Clinical Research Associate will support a study in the cardiovascular/electrophysiology medical device space, specifically focusing on A-fib indication. This involves monitoring experience, applying in-depth knowledge of regulations, and implementing solutions for site issues.
This is a resume drop-off for future opportunities within the Design/Research or Content Strategy teams at Nava, a consultancy focused on modernizing government technology services. Applicants should submit their resume and portfolio for future review against role qualifications.
The facilitator will guide students through interactive online sessions to deliver curriculum content, support assessment tasks, and provide constructive feedback on student submissions while upholding academic integrity. This role also involves participating in program coordination meetings and handling administrative tasks related to the modules facilitated.
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
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The primary responsibility is to build and lead a world-class research operation that consistently generates early, differentiated insight across public and private markets. This involves architecting high-performance teams, designing intelligence pipelines, and partnering with the Principal to shape the firm's worldview.
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to ethical principles. Responsibilities also include coordinating scheduling, managing participant inquiries, recording session notes, and following up with written action plans and resources.
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to protocol. This includes coordinating scheduling, maintaining rapport, recording sessions, and following up with resources and action plans.
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