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Develop and execute the APAC regional sales strategy to drive revenue growth and expand market share for health research solutions. Lead and coach a geographically distributed sales organization while managing executive-level relationships with key institutional customers.
Lead the technical vision and strategy for off-platform and evidence personalization, focusing on GenAI-powered messaging and asset creation. Drive cross-functional partnerships to design and ship scalable production ML systems that increase member engagement and revenue.
The role involves managing large neuroimaging datasets and developing reproducible computational pipelines on high-performance computing systems. Additionally, the associate will support the PI with the UKB-RAP environment and handle IRB and Data Use Agreement documentation.
Architect, scale, and optimize scientific codebases to power Large Quantitative Models for drug and materials discovery. Transition high-impact research prototypes into robust, production-grade software and orchestrate distributed training pipelines on GPU infrastructure.
Lead and supervise the programming and research of fund tax loss harvesting processes for fixed income, equity, and mixed funds. This includes developing scalable data tools and optimizing client accounts using statistical modeling.
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Develop fault-tolerant quantum solutions and core IP to solve complex real-world problems across various industry verticals. Collaborate with internal and external partners to define quantum workflows and represent the company at technical conferences.
Oversees the execution of clinical trials at investigative sites, acting as a liaison between the sponsor and sites to ensure data integrity and participant safety. Responsibilities include site initiation, monitoring, close-out, and mentoring junior staff.
The Medical Director will lead the design and execution of clinical trials for the endocrinology portfolio, contributing to the Concise Clinical Development Plan (CCDP). They will provide medical monitoring, oversee regulatory documentation, and represent the company to academic and regulatory organizations.
Provide consultative support and expert advice to higher education and K-12 executives on advancement and fundraising strategies. Deliver high-impact presentations and workshops to help partners implement best practices and achieve strategic goals.
Provide consultative support and expert advice to senior higher education leaders on advancement, fundraising, and institutional strategy. Deliver high-impact presentations and workshops to help partners implement best practices and drive strategic progress.
Provide expert legal and non-legal research, reference, and document retrieval services to attorneys and staff. Monitor legislative developments and provide strategic guidance on research methodologies to ensure efficiency.
The role involves managing site and supervisory activities for assigned oncology studies for a single dedicated client. Responsibilities include monitoring sites and mentoring junior Clinical Research Associates.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.
Conduct outbound calls to interview and recruit respondents for market research studies using scripted questionnaires. Accurately record participant responses in Excel databases and invite qualified individuals to focus groups.
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Lead the end-to-end research strategy for web and eCommerce platforms to drive customer-centered decision-making across cross-functional teams. Establish research operations and translate complex findings into actionable recommendations to improve business outcomes and user experience.
The intern will join the Clean Air Team to support a growing portfolio of behaviour change initiatives. They will contribute to research and impact at scale within the field of public policy.
The role involves operationally coordinating a clinical research study on obesity interventions and designing a 6-week autonomy-supportive group coaching series. Additionally, the coordinator will deliver live virtual coaching sessions to participants and manage study documentation and data collection.
Provide technical coaching in equity research strategy, financial analysis, and valuation to help clients land or grow in research roles. Support clients with career development, including resume reviews, interview prep, and networking strategies.
The role involves building and optimizing dashboards to monitor audience behavior and platform performance across digital portfolios. You will synthesize large datasets into actionable insights to support distribution negotiations and business growth.
The CRA I supports the research team by managing study startup, implementation, and closeout activities. Key duties include coordinating research data, handling regulatory submissions, and interacting with patients for informed consent and data collection.
Serve as the Principal Investigator for a multimodal survey experiment testing hybrid designs against Demographic and Health Surveys in West and Central Africa. Lead the scientific design, implementation, analysis, and dissemination of findings while managing a multidisciplinary team and international partners.
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Lead the strategic direction and operational excellence of end-to-end billing and revenue cycle services, specifically overseeing Patient Research and Call Center teams. Ensure compliant, efficient billing operations that maximize reimbursement and minimize revenue leakage for EMS clients.
Lead the Advancement terrain by providing expert consultative advice and strategic guidance to higher education executives. Manage a team of advisors while collaborating with research and sales teams to drive client success and institutional transformation.
Manage research activities at clinical sites, including site identification, start-up, and close-down. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and safety reporting requirements.
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