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The intern will conduct online legal research on human rights and environmental lawsuits and contribute to the Just Transition Litigation Tracking Tool. Additionally, they will draft updates for the CLA Quarterly newsletter and perform routine data entry tasks.
The Research Analyst will own the end-to-end research process, from identifying relevant topics and analyzing data to producing institutional-grade reports. They will collaborate with editorial, product, and commercial teams to develop high-quality research products and insights.
You will own, build, and run your own startup in the AI research field while receiving intensive coaching and support. You will iterate your product to achieve product-market-fit and build out your sales and marketing operations.
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You will own, build, and run your own startup within the AI research lab sector. You will also participate in an intensive personal development program and receive support in scaling your business and securing funding.
The role involves conducting deep market research and customer intelligence to provide actionable insights. You will utilize various tools and AI technologies to support account research and strategic decision-making.
The Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage site relationships, and support the clinical team in delivering quality research outcomes.
You will conduct clinical trial monitoring activities including site visits, protocol compliance, and data integrity maintenance. Additionally, you will collaborate with investigators and site staff to facilitate study conduct and prepare clinical study documentation.
You will set the research agenda and write flagship reports while managing editorial standards across all company publications. Additionally, you will lead policy engagement and build data-driven narratives to influence the debate on labour market regulation.
Lead the operational execution of global medical device clinical studies from start-up through close-out. Manage investigative sites to ensure protocol compliance, data quality, and effective risk mitigation.
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 documentation.
The Associate Director manages a team of 6-14 Clinical Research Associates to ensure clinical trial performance and adherence to regulatory standards. They are responsible for resource allocation, staff development, and resolving operational issues at clinical sites.
This position is responsible for implementing statewide research projects focused on sport fish management and supervising research technicians and interns. The role involves analyzing complex research data, preparing technical reports for publication, and providing scientific expertise to support wildlife management.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol and regulatory compliance. You will conduct remote or on-site visits to assess data accuracy, manage documentation, and resolve site-related issues.
Support clinical research projects across operational functions by preparing and tracking study documents, training, endpoint testing, data queries, and user access. Coordinate with sites, sponsors, and internal teams to resolve issues, complete deliverables on time, and follow applicable procedures and regulations.
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The manager will design and execute an impact measurement system to evaluate the MicroBuild Initiative's outcomes and institutional changes. They are responsible for commissioning independent research, managing the evaluation budget, and communicating findings to stakeholders to drive evidence-based decision-making.
The intern will develop efficient methodologies and prototype solutions for self-evolving vision foundation models and vision-language models. They will collaborate with research and engineering teams to translate research into practical solutions for cloud and edge deployment.
Conduct technical assessments of emerging AI models for dual-use biological risks, including running evaluation pipelines, analyzing model behavior, and assessing biological knowledge and willingness. Synthesize findings into reports and risk summaries for AI developers and regulatory bodies, and contribute to research papers and public capability-trend resources.
The Clinical Research Associate is responsible for monitoring clinical trial activities, including site initiation, recruitment, and data quality, in accordance with GCP and ICH standards. They manage site performance, facilitate regulatory submissions, and ensure study milestones are met through regular communication and training.
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 local regulations. They act as the main point of contact for clinical trial teams and lead local study teams to ensure high performance and adherence to quality standards.
The Research Director will own client relationships and create research strategies to embed data into client workflows while driving account growth. They will also manage large, complex research projects and mentor team members to ensure high-quality delivery and strategic insights.
The Initiation Clinical Research Associate leads and executes study start-up, site activation, and regulatory submission activities. They act as the primary contact for assigned sites to ensure compliance and maintain high-quality documentation throughout the study lifecycle.
The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They provide project management oversight, including budget, risk, and milestone management, while maintaining high-quality client service.
The Research Analyst Engineer is responsible for researching, gathering, and organizing technical hardware and software specifications for internal databases. They will also fact-check data, edit content for web publication, and ensure all information meets quality guidelines.
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Design and implement optimization models and a production-grade scheduling solver for workforce planning, scheduling, and resource allocation in a large-scale contact center environment. Validate schedule quality and solver performance, integrate the service into the WFM platform, and collaborate with business and engineering stakeholders to ensure schedules are operationally usable.
Support the finalization of the TIFA-TCG evaluation by reviewing documents, extracting evidence, managing stakeholder comments, refining analysis, and assisting with targeted consultations. Help quality-check report materials, revise and format the report, manage data and references, and provide administrative coordination.
Manage site activities and supervise assigned oncology studies for a dedicated client, including independent monitoring across all types of visits. Collaborate with sponsors and subject matter experts, and mentor junior CRAs as appropriate.
The Associate Director will drive clinical research and real-world evidence generation activities to support product development, regulatory submissions, and market access. They will collaborate with cross-functional teams to design study protocols, interpret clinical data, and manage scientific communications.
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