The Field Supervisor is responsible for recruiting, hiring, and managing a team of test administrators to ensure the successful implementation of school-based assessments. They must also monitor project performance, provide staff training, and maintain clear communication with project management.
The medical editor will edit scientific deliverables for grammar, style, and consistency while ensuring high-quality standards across various formats like manuscripts and posters. They will collaborate with writers, researchers, and designers to manage production schedules and ensure accurate graphical representation of data.
The analyst will coordinate and assist on evidence synthesis projects, including systematic reviews, scoping reviews, and health technology assessments. They will also manage research data, conduct literature searches, and support the development of research products like reports and manuscripts.
The Research Programmer/Analyst will collaborate with research teams to analyze and synthesize complex healthcare data using Python, SAS, or SQL. They will also provide technical leadership, mentor early-career staff, and implement best practices for analytic programming and quality assurance.
The Programmer/Analyst will develop and maintain Python or SQL code to query, merge, and analyze complex healthcare data from large relational databases. They will collaborate with research teams to transform disparate data sources into meaningful analytic insights for reports and manuscripts.
The engineer will develop and calibrate hydrologic, hydraulic, and reservoir models to support flood risk assessment and integrated water resources planning. They will also collaborate with multidisciplinary teams to create computational tools and communicate technical findings to various stakeholders.
The Traveling Field Interviewer is responsible for recruiting participants, conducting in-home interviews, and collecting confidential health and dietary data. They must independently manage administrative tasks, maintain project equipment, and travel frequently to various locations to meet study requirements.
The Manager of Oracle Technologies will lead a team of integration engineers and developers to design, build, and maintain technical integrations for Oracle Cloud and enterprise business systems. This role involves overseeing vendor relationships, establishing architectural governance, and driving the adoption of AI-assisted orchestration within the Oracle platform.
The Principal Investigator serves as the overall project leader for multi-site clinical research coordinating centers, overseeing study design, implementation, and quality control. They are responsible for managing contractual and fiscal aspects, leading business development, and mentoring junior staff while maintaining relationships with funding agencies and steering committees.
The Investigator/Research Epidemiologist serves as a member of the leadership team for coordinating centers of multi-site clinical research projects. They oversee operational and scientific aspects including study design, protocol development, data analysis, and business development activities.
Collaborate with research teams to design, implement, and maintain informatics solutions for clinical and epidemiological studies. Provide technical support, manage data collection strategies, and ensure high-quality standards across research projects.
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.
The role involves assisting with quantitative research activities such as data analysis, statistical modeling, and the preparation of technical reports. Additionally, the position requires contributing to project management tasks and conducting literature reviews to support health policy research.
The Associate Director will lead the planning and execution of statistical analyses for clinical trials and observational studies, with a focus on patient-reported outcomes. They will also oversee project teams, contribute to proposal development, and provide methodological solutions to cross-functional stakeholders.
The specialist will provide leadership and subject matter expertise for FDA-regulated clinical research, ensuring compliance, risk management, and inspection readiness. They will oversee quality management processes, manage CAPA workflows, and support clinical trial infrastructure across various research programs.
Lead multidisciplinary teams in the design and execution of patient-centered outcomes research to support pharmaceutical and biotechnology clients. Serve as a scientific leader and working manager, overseeing study design, regulatory engagement, and the dissemination of research findings.
Lead and grow the Evidence Synthesis & Statistics capability by providing strategic, scientific, and operational leadership. This role involves delivering complex analytical work for global clients while driving business development and mentoring a high-performing team of statisticians.
