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The analyst will conduct and publish forensic accounting research on U.S. listed healthcare companies to identify financial risks and operational issues. They will also manage client inquiries, maintain industry dashboards, and deliver research findings through reports and presentations.
The Senior Research Assistant will co-lead client onboarding for the IAMRARE Registry Program and provide ongoing technical support and platform training. They will also manage study documentation, conduct quality assurance testing, and coordinate logistics for partner meetings and webinars.
You will lead the research and thought leadership program by identifying data-driven stories and turning them into high-quality, cross-channel marketing campaigns. You will collaborate with executive leadership to shape the brand voice and ensure all content aligns with product strategy and market trends.
The Senior Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data queries, and overseeing drug accountability.
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits and ensuring compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing clinical documentation, and overseeing drug accountability throughout the trial lifecycle.
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The In-House Clinical Research Associate II is responsible for managing clinical study sites in accordance with GCPs and regulatory requirements. They provide support to project teams, maintain study documentation, and assist with remote monitoring and data management tasks.
Lead complex market research projects from planning through delivery to support product strategy and business growth. Analyze large datasets and synthesize findings into actionable recommendations and clear visualizations for business leaders.
The Senior Clinical Research Associate serves as the primary point of contact for investigational sites, conducting monitoring visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for overseeing patient safety, managing site documentation, and ensuring high-quality data entry throughout the clinical trial process.
The Clinical Research Associate is responsible for monitoring clinical trial sites to ensure compliance with protocols and regulatory requirements. They will oversee site activities, manage data integrity, and ensure the safety and well-being of study participants.
The Research Nurse Trainer is responsible for developing, administering, and tracking compliance for education and training programs for research staff and investigators. They also collaborate with clinic management to facilitate protocol-specific training and assist in the development of education-based corrective action plans.
The Senior Clinical Research Associate is responsible for performing investigative site management and monitoring activities to ensure data integrity and subject safety throughout the clinical trial lifecycle. They will act as the primary contact for sites, facilitate communications, and support regulatory inspections while maintaining inspection readiness.
The analyst will manage product catalog integrity, accuracy, and quality across various e-commerce platforms and internal CMS tools. They will also optimize product listings for SEO and support digital merchandising strategies through continuous research and performance analysis.
The role involves labeling and curating clinical data to train AI models and performing human-in-the-loop evaluations to ensure clinical accuracy and safety. You will also engage in prompt engineering and develop scoring rubrics to refine AI performance in healthcare applications.
The role involves labeling and curating clinical data to train AI models while performing human-in-the-loop evaluations for accuracy and safety. You will also design prompts, refine scoring rubrics, and collaborate with researchers to improve clinical annotation standards.
You will be responsible for all site management and supervisory activities for oncology studies while working with industry leaders. Additionally, you will mentor junior CRAs and ensure compliance with clinical research guidelines.
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The Research Nurse will coordinate patient care and facilitate communication between patients and healthcare providers to ensure study protocol compliance. They are responsible for monitoring patient progress, collecting accurate data, and providing individualized support throughout the clinical research process.
The Clinical Research Physician participates in the development, conduct, and reporting of global clinical trials to support product registration and commercialization. They serve as a scientific resource for study teams, ensuring compliance with regulatory standards and managing medical strategies for marketed compounds.
You will support the end-to-end execution of complex, mixed-methods user research studies from setup to delivery. This includes collaborating with senior team members to synthesize data, uncover trends, and produce client-ready reports.
The intern will conduct market research on private capital formation and build a pipeline of exciting businesses for potential investment. Responsibilities include first-pass screening of companies, writing investment notes, and tracking regulatory changes across various jurisdictions.
You will lead complex Global Vulnerability Management workstreams and advance the company's Threat Exposure Management capabilities. Additionally, you will conduct hands-on vulnerability research, perform security validation, and partner with cross-functional teams to mobilize remediation efforts.
The Senior Clinical Research Scientist will conceptualize research questions, design studies, and perform advanced statistical analyses to generate clinical and economic evidence for Omada's programs. This role involves collaborating with cross-functional teams to translate research findings into value narratives and commercial assets for diverse stakeholders.
Provide subject matter expertise in statistical analysis to support Air Force accession conditions, readiness, and long-term health outcomes. Manage analytical projects, develop statistical models, and draft technical documentation for internal and external stakeholders.
The Project Director provides operational leadership and oversight for clinical research projects, ensuring delivery within scope, budget, and quality standards. They are responsible for managing cross-functional teams, driving business development, and maintaining strong client relationships.
The research assistant will administer standardized reading assessments for a middle school intervention project and ensure accurate scoring and documentation. They will work as part of an assessment team to gather data while maintaining strict student confidentiality and project protocols.
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The Senior Director will manage the ALS Association's research program, overseeing funding initiatives, grant reviews, and scientific strategy. They will also build relationships with research leaders, biotechnology partners, and donors to advance drug development and scientific goals.
The Research Associate will conduct quantitative data management and analysis, including literature reviews and the development of research questions to support clinical and operational projects. They will also identify grant funding opportunities and translate complex findings into actionable insights for both scientific and non-technical audiences.
The Associate Director will influence commercialization strategies by designing and executing primary market research projects for the oncology pipeline. They will collaborate with cross-functional teams to translate research findings into actionable insights that support data-driven decision-making.
The Director will lead research, evaluation, and impact storytelling for K-12 global education products by turning program data into evidence-based narratives. They will manage research projects, ensure data governance compliance, and collaborate with sales and marketing teams to communicate program impact to partners.
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