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Participants will engage in various research activities such as completing online questionnaires, participating in remote discussions, and testing new concepts. They will provide feedback on products and services to assist in market research studies.
The Clinical Research Associate oversees clinical trial sites to ensure quality, integrity, and compliance with protocols, SOPs, and regulatory guidelines. They conduct site visits, monitor data accuracy, and maintain effective relationships with internal and external stakeholders to meet study objectives.
The Medical Director will serve as the primary clinical partner for biopharma accounts, bridging clinical practice with real-world data and AI-driven solutions. They are responsible for developing long-term clinical strategies, analyzing client pipelines, and providing expert guidance on trial protocol design and market needs.
The Clinical Research Associate coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-related issues.
The Principal Research Analyst leads the development and delivery of high-quality content, guidance, and practitioner aids for information security. They also serve as a subject matter expert, mobilizing volunteer groups and representing ISACA at industry events and conferences.
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Participants will engage in various research activities such as completing online questionnaires, participating in remote discussions, and testing concepts. They will also provide feedback on products and services through surveys, interviews, and focus groups.
The Research Manager will develop and execute the organization's research agenda by managing contract researchers and partner academics to produce actionable guidance. They will also oversee the end-to-end publication pipeline, ensuring research outputs are effectively delivered to AI company insiders and partners.
The Research Associate II manages and implements research studies and evaluation projects while contributing to data analysis and reporting. They also conduct data collection activities such as surveys, interviews, and focus groups while maintaining project timelines and deliverables.
The Research Representative is responsible for researching and resolving member eligibility verification requests while maintaining high production and accuracy standards. They must also manage documentation in internal systems and provide professional customer service to members and providers.
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 market research.
The Clinical Research Associate is responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. They also ensure the protection of study patients, verify protocol adherence, and maintain the integrity of data submitted on Case Report Forms.
The Medical Director will lead clinical development programs for neurology assets, overseeing study design, protocol development, and execution. They will serve as the internal medical monitor, collaborate with cross-functional teams, and contribute to regulatory filings and scientific presentations.
The Senior Clinical Research Associate manages and monitors clinical studies from start-up through closeout to ensure compliance with protocols and regulatory standards. They collaborate with investigative sites, CROs, and cross-functional teams to maintain data quality and patient safety.
The fellow will conduct research and design projects focusing on the cultural landscape of a historic property, including assessments of garden conditions and climate change impacts. They will also develop restoration recommendations, maintenance plans, and graphic reports on historical weather impacts on local tree communities.
The role involves fine-tuning LLMs for translation tasks and building evaluation pipelines to ensure high-quality language output. You will also develop agentic workflows and collaborate with cross-functional teams to integrate research into production systems.
You will design, train, and evaluate LLMs for translation and language-quality tasks while building agentic workflows for multi-step reasoning. You will also own a significant research workstream, collaborating with cross-functional teams to integrate research findings into production systems.
Lead a high-performing applied science team to develop and deliver transformative agentic AI solutions for tax and accounting professionals. Partner with product engineering and domain experts to transition research innovations into scalable, production-ready capabilities that improve customer workflows.
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The research assistant will support the Principal Investigator by transcribing and coding qualitative and quantitative data while performing basic statistical analyses. They will also contribute to literature reviews, manage participant data, and utilize LLMs to develop automated coding tools.
The Clinical Research Writer will build and lead a structured clinical research function, organizing research efforts across programs. They will analyze clinical and operational data to develop abstracts, manuscripts, and peer-reviewed cardiovascular publications.
You will build and improve AI systems and pipelines that power the company's core platform, including SearchAI, ZoneAI, and SiteAI. Your work involves scaling inference, processing large-scale geospatial data, and shipping production-quality code to integrate research outputs into the platform.
Participants will engage in various research activities such as completing online questionnaires, joining remote discussions, and testing concepts. They will also provide feedback on products and services as part of an online research panel.
The Clinical Research Associate is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with investigators to facilitate study conduct and perform data review to maintain high-quality clinical data.
The Senior Project Manager will lead and manage global qualitative market research projects from proposal acceptance through final invoicing. They will serve as the primary client contact while coordinating with internal teams to ensure high-quality, budget-compliant project delivery.
The Research Administrator leads and supervises staff performing pre-award activities, including budget development and proposal submission for sponsored projects. They also ensure compliance with federal regulations, mentor team members, and coordinate with post-award teams to facilitate research operations.
The role involves ensuring the quality and timely submission of clinical trial data and managing regulatory and ethical documentation. You will also perform site identification activities and maintain site-related documentation within the Trial Master File.
You will lead the research and design function, setting the strategic vision for both consumer and B2B products to ensure a cohesive user experience. You are responsible for building a high-quality design system, managing the research team, and aligning product design with the company's brand identity.
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The Clinical Research Associate II will contribute to the development of therapies by supporting clinical trials and regulatory processes. They will work to improve global health outcomes through the delivery of clinical development solutions.
The Senior CRA is responsible for site qualification, initiation, monitoring, and close-out visits in accordance with GCP and regulatory standards. They also provide mentoring to less experienced staff, coordinate global study activities, and ensure the quality and timely submission of clinical data.
The Clinical Research Associate acts as the primary site contact and manager, ensuring study conduct aligns with ICH-GCP, local regulations, and company quality standards. They are responsible for site monitoring, data integrity, and managing regulatory documentation throughout all phases of clinical research studies.
Fellows will conduct research on technology trends, AI, and cloud infrastructure to support the development of newsletters, articles, and industry briefs. They will also summarize complex topics into clear, executive-facing content for Fitzroy Consulting.
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