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The Director of Business Development will identify, develop, and close revenue-generating opportunities and strategic partnerships within the North American pharma, biotech, and academic sectors. They will manage a balanced portfolio, forecast quarterly revenues, and collaborate across internal teams to drive growth for the Research Solutions & Strategic Partnerships unit.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance throughout the study.
LINC Fellows provide subject matter guidance, academic support, and assessment marking for postgraduate nursing students. They are responsible for managing discussion forums and providing proactive, personalized support to student queries.
The LINC Fellow will provide subject matter guidance, academic support, and assessment marking for a group of 25-30 online students. They are responsible for conducting 1:1 sessions, managing discussion forums, and providing personalized support to student queries.
The Clinical Research Associate oversees clinical trial sites to ensure quality, integrity, and compliance with protocols and regulatory standards. They conduct monitoring visits, manage site relationships, and perform data verification to ensure patient safety and data reliability.
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This position coordinates industry-sponsored clinical research invoicing, billing, and reconciliation activities to ensure earned revenue is realized. It also provides training and guidance to study teams on the use of clinical trial management systems for financial tracking.
The student researcher will assist the Ecampus Research Unit by coding qualitative data, performing quantitative analysis, and creating visual data displays. They will also contribute to scholarly writing, literature summaries, and report development while attending weekly team meetings.
Design, implement, and operate high-impact machine learning models to drive member growth and monetization. Collaborate with cross-functional teams to translate business intuition into scalable, production-ready data-driven solutions.
The Research Assistant will oversee data collection, organization, and management for the MOVED study, including conducting in-person survey interviews and physical health measurements at participants' homes. They will also assist the research team with data cleaning, report generation, and literature searches to support policy briefs.
The Senior Research and Data Analyst is responsible for the development, collection, and maintenance of data assets and reporting systems, including quality and financial metrics. The role also involves mentoring junior staff and collaborating with technical leaders to enhance data operations and services.
The Research Manager will track and analyze the global datacenter market, including facilities, equipment, and services. They will also produce structured reports, present at industry events, and collaborate with other analysts to align infrastructure datasets.
The Research Assistant will coordinate administrative and programmatic research projects, including data analysis, literature reviews, and stakeholder meeting management. They will also support the development of research resources and maintain effective communication across internal teams and external partners.
Research assistants will support faculty by screening participants, conducting clinical interviews, and managing research data. They are also responsible for performing qualitative or quantitative analysis and maintaining accurate subject records.
The Senior Clinical Research Associate implements and monitors clinical trials to ensure compliance with regulatory requirements and ICH GCP guidelines. They are responsible for site startup activities, data verification, and facilitating the timely resolution of clinical trial issues.
The Senior Clinical Research Associate implements and monitors clinical trials to ensure compliance with regulatory requirements and GCP guidelines. They are responsible for site startup activities, data verification, and facilitating the resolution of clinical trial issues.
The researcher will produce an original 50-page paper examining how climate policies with global consequences can be developed through inclusive processes. The work involves identifying concrete institutional and methodological approaches for meaningful participation of Global Majority actors in climate policymaking.
Deliver product experiences on the T1 AI and networking platforms while collaborating with design and product management. Act as a product owner to build and innovate on the front-end architecture and design system.
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The Senior Clinical Research Associate will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Responsibilities include monitoring clinical sites, conducting site visits, collaborating with cross-functional teams, and providing training to site staff.
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring compliance with FDA and ICH-GCP regulations, and managing regulatory documentation. Additionally, the role involves performing data verification, assisting with budget negotiations, and mentoring junior team members.
The Research Director provides strategic and operational leadership for core research functions, including data, tools, and participatory research. They manage a multidisciplinary team, oversee research integrity, and ensure the delivery of actionable analysis to mitigate political violence.
The Research Associate will conduct epidemiological analysis, model program impact and cost-effectiveness, and monitor the success of health interventions. They will collaborate with country teams to identify priority programs and provide evidence-based insights to inform resource allocation.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They collaborate with study teams and sponsors to maintain protocol compliance and manage investigational product accountability.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with company policies and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data integrity and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with regulatory requirements and SOPs. They will ensure subject safety, data integrity, and protocol compliance while collaborating with study teams and sponsors.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They will collaborate with study teams and sponsors to manage investigational products and maintain compliance with GCP and regulatory requirements.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They will collaborate with study teams and sponsors to manage investigational products and maintain compliance with regulatory requirements and SOPs.
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The Research Officer will collect and analyze farm business data to produce accurate annual accounts and industry reports. This role involves conducting interviews with farmers and traveling to various farm locations to gather financial and operational information.
You will lead end-to-end research and development of a foundation model for construction drawings, from architecture design to production deployment. This involves running rigorous experiments, collaborating with cross-functional teams, and shipping high-accuracy models to real customers.
The analyst will support Army logistics and materiel management programs by conducting inventory analysis, supply chain research, and strategic planning. They are responsible for synthesizing complex data into executive-level briefings and reports to facilitate informed decision-making.
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. Responsibilities include conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
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