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The consultant will manage projects and lead teams to drive organizational effectiveness and strategic initiatives within academic medical centers. They act as a primary liaison between the client and the firm, fostering relationships while delivering insightful analysis and technology solutions.
The intern will support the ADAS research team in developing functions and reinforcement learning algorithms. They will work on cutting-edge research challenges in autonomous driving, including multi-agent self-play and Python script development.
The intern will support the ADAS research team by developing new functions and collaborating on reinforcement learning algorithms. Responsibilities include working on autonomous driving research topics such as multi-agent self-play and creating Python scripts for benchmarking and APIs.
The Clinical Research Associate will conduct site monitoring activities, including qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with site staff and investigators to maintain high-quality clinical data and prepare essential study documentation.
The Research Director will lead the NAVLIN policy services team, overseeing the production of policy intelligence, news services, and MFN tracking. They will also act as a senior client-facing expert, driving business development and integrating AI-driven analytics into service offerings.
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The analyst will independently manage research workstreams and projects focused on global renewable energy markets, including photovoltaics and battery storage. They will also produce high-quality market intelligence reports, maintain structured databases, and collaborate with international teams to support client solutions.
The Portfolio Leader will develop and manage the research reagents product portfolio by conducting competitive research, customer segmentation, and strategic growth planning. They will also provide training and support to global sales teams while collaborating cross-functionally to achieve business objectives.
The Senior Clinical Research Associate coordinates site identification, feasibility assessments, and monitoring activities to ensure compliance with regulatory requirements and protocols. They also manage site budgets, contracts, and essential documentation while training site personnel to ensure trial quality and adherence to deadlines.
The Data & Research Lead will manage Canopy's data, research, and technical knowledge systems while coordinating research across the Impact team. This role involves setting data governance standards, overseeing decision-support tools, and leading a team of researchers and specialists.
Participate in various research studies to contribute to meaningful outcomes. Perform data entry tasks while following oral and written instructions.
The Field Clinical Research Associate III manages clinical study sites to ensure protocol compliance, high-quality data collection, and audit readiness. They also collaborate on study documentation, provide mentorship to junior staff, and act as a liaison between the company and investigational sites.
The intern will support the Global Commercial Vehicle Drive to Zero program by maintaining and updating the OZETI and ZETI databases. They will also assist in researching high-potential organizations for future partnerships and provide data analysis for stakeholder engagement.
The Senior Research & Analytics Scientist provides scientific leadership for patient experience measurement products and benchmarking programs. This role ensures methodological rigor, develops governance frameworks, and translates complex data into actionable insights for healthcare improvement.
The Clinical Research Regulatory Specialist will lead the implementation and optimization of the electronic regulatory (eRegulatory) platform while serving as the primary liaison between research teams and technology partners. They are responsible for ensuring regulatory compliance, managing essential study documentation, and providing training and support to research staff.
The Clinical Research Regulatory Specialist will lead the implementation and optimization of an electronic regulatory platform while serving as the primary liaison between research teams and leadership. They are responsible for ensuring regulatory compliance, managing essential study documentation, and providing training to research staff on digital workflows.
The Field Senior Clinical Research Associate manages clinical site monitoring activities to ensure compliance with Good Clinical Practice and regulatory guidelines. They serve as the primary point of contact for investigative sites, supporting study start-up, enrollment, and data management tasks.
The Clinical Research Associate II will conduct site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They will also collaborate with investigators and site staff while performing data review to maintain high-quality clinical study documentation.
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The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing safety reporting, and conducting study initiation visits.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure regulatory compliance and data integrity while overseeing site performance throughout the study lifecycle.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and regulatory compliance. They will conduct study initiation visits and oversee site performance throughout the duration of the clinical trials.
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They are responsible for ensuring regulatory compliance, managing informed consent, and overseeing safety reporting throughout the study lifecycle.
The Clinical Research Associate is responsible for all aspects of site monitoring and management, including routine monitoring visits, site closeouts, and ensuring protocol adherence. They also manage study documentation, vendor interactions, and data integrity while maintaining audit readiness at the site level.
The HEOR Lead will translate clinical and real-world evidence into defensible economic value for payers and employers. They will develop budget-impact, cost-effectiveness, and ROI models to support healthcare growth and evidence investment.
The role involves conducting extensive data research on the telecommunications industry and managing data aggregation using Excel. You will support client tactical decisions by monitoring provider marketing strategies and maintaining high-quality research standards.
The Research Analyst will conduct due diligence research using internet and proprietary databases to produce high-quality reports on companies and individuals. They will also perform watchlist screening and collaborate with global teams to ensure report accuracy and timeliness.
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Conduct due diligence research using internet and proprietary databases to produce high-quality reports on companies and individuals. Collaborate with regional teams to ensure report accuracy, timeliness, and adherence to company standards.
Conduct in-depth research using internet and web-based media databases to produce high-quality due diligence reports. Ensure all reports meet strict standards for accuracy, timeliness, and completeness while collaborating with global teams.
The analyst will author syndicated research reports, market forecasts, and articles covering various automotive technologies and adjacent markets. They will also work on custom research projects, maintain industry relationships, and support sales and business development efforts.
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