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The Research Specialist 2 will implement community-based mixed methods evaluation protocols, manage data collection, and assist in report generation. They will also supervise qualitative data collection, maintain project databases, and facilitate meetings with project team members.
The Associate Director will drive lead generation and manage the full sales cycle from prospecting to closing new business. They will also build and nurture relationships with key decision-makers at pharmaceutical, biotech, and CRO organizations.
The Research Fellow will participate in a research program under the guidance of a Mayo Clinic principal investigator. The role focuses on gaining training and education in research while working toward becoming competitive for national research grants.
The Content Research Lead will design and execute sponsor-funded quantitative research projects and manage the production of high-impact editorial content. They will also oversee client relationships, host live events, and collaborate with sales teams on research-driven proposals.
Drive revenue growth for AI-powered research intelligence platforms by building strategic partnerships with academic institutions. Manage the full sales cycle, including pipeline management, consultative selling, and representing the company at academic conferences.
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Drive revenue growth for AI-powered research intelligence platforms by managing strategic partnerships with academic institutions. Develop and execute account strategies while utilizing consultative sales techniques to address the needs of university leaders and researchers.
The role involves coordinating clinical trial monitoring activities, maintaining study documentation, and ensuring compliance with protocols and regulatory requirements. You will also manage sponsor queries, monitor study cost efficiency, and build collaborative relationships with clinical investigators and site staff.
You will coordinate clinical trial monitoring activities, maintain study documentation, and ensure compliance with protocols and regulatory requirements. Additionally, you will build collaborative relationships with stakeholders and investigators to ensure high-quality clinical outcomes.
You will independently coordinate clinical trial monitoring activities, maintain study documentation, and ensure compliance with protocols and regulatory requirements. Additionally, you will manage sponsor queries, optimize study cost efficiency, and foster collaborative relationships with clinical investigators and site staff.
The role involves coordinating clinical trial monitoring activities, maintaining study documentation, and ensuring compliance with protocols and regulatory requirements. You will also manage sponsor queries, monitor study cost efficiency, and build collaborative relationships with clinical investigators and site staff.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will interpret complex medical data and collaborate with site staff to maintain high-quality clinical documentation.
You will independently coordinate clinical trial monitoring activities, maintain study documentation, and ensure compliance with protocols and regulatory requirements. Additionally, you will manage sponsor queries, monitor study cost efficiency, and foster collaborative relationships with site staff and investigators.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
The Clinical Research Associate II is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with investigators and site staff while contributing to the preparation of study documentation and clinical study reports.
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, manage informed consent processes, and oversee safety-related event reporting.
Participants will engage in various research activities such as completing online questionnaires, participating in remote discussions, and providing feedback on products. These activities are voluntary and based on individual availability and study relevance.
Participants will engage in various research activities such as completing online surveys, participating in interviews, and joining focus groups. They will also provide feedback on products and services to assist in research studies.
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Participants will engage in online research activities such as surveys, interviews, and focus groups. They will provide feedback on various products and services to assist with research objectives.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data reviews to maintain high-quality clinical documentation.
You will conduct clinical trial site visits including qualification, initiation, monitoring, and close-out to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data review to maintain high-quality clinical documentation.
The Clinical Research Associate will conduct site qualification, initiation, monitoring, and close-out visits while ensuring protocol compliance and patient safety. They will also collaborate with investigators and site staff to maintain high-quality clinical data and prepare study documentation.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits. Additionally, you will ensure protocol compliance, maintain data integrity, and collaborate with investigators to facilitate study conduct.
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 data.
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 data.
Responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and maintenance of study files. Ensures patient protection, protocol adherence, and data integrity through careful source document verification and CRF review.
The CRA 2 is responsible for all aspects of study site monitoring, including routine monitoring, site management, and ensuring protocol adherence. They also manage registry tasks, process Serious Adverse Event reports, and maintain data integrity within electronic systems.
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Participants will engage in various research activities such as completing online questionnaires, participating in interviews, and joining focus groups. They will also provide feedback on products and services as requested by the research panel.
Participate in a virtual career event to learn about the daily experiences and professional journeys of Citi analysts and associates. Engage with industry professionals to gain insights into the Markets & Research sector and prepare for a career transition.
The role involves assisting with quantitative research activities, including data analysis, statistical modeling, and the preparation of technical reports. Additionally, the incumbent will contribute to project management tasks and conduct literature reviews to support health policy research initiatives.
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