Lead and mentor a team of health economists while serving as a technical and strategic lead on client projects involving economic modeling, data analysis, pricing, reimbursement, market access, and health technology assessment submissions. Oversee project quality and delivery, support staffing and operational planning, improve processes, and contribute to proposals, marketing, and conference activities.
The role involves acting as a financial co-pilot for project managers to drive project profitability and financial health while leading and coaching a team of India-based financial analysts. You will be responsible for managing the monthly forecasting cycle, performing variance analysis, and ensuring high-quality financial support across the business.
The Principal Statistical Programmer will independently generate SDTM and ADaM datasets, specifications, and complex statistical outputs for clinical trials. They will also oversee CRO programming deliverables and ensure compliance with FDA regulations and clinical development standards.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials using SAS while ensuring compliance with CDISC standards. They will also generate and validate datasets, tables, listings, and figures, and support submission documentation for regulatory purposes.
The role involves designing and delivering fit-for-purpose data and analysis infrastructure platforms to support clinical trial data flow. It also requires collaborating with internal teams to develop reusable R packages and utilities while promoting technical innovation in clinical data environments.
The Senior Revenue Accountant will own global revenue recognition and reporting, ensuring compliance with ASC 606 and US GAAP standards. They will also collaborate with cross-functional teams to complete month-end close activities, account reconciliations, and process improvements.
The Senior Clinical Data Manager is responsible for performing ongoing data review to ensure the accuracy, completeness, and consistency of clinical trial data. They will collaborate with cross-functional teams to resolve discrepancies and manage database lock activities in compliance with regulatory standards.
Lead and support advanced real-world evidence analyses to inform clinical development, regulatory strategy, and HEOR decisions. Develop and implement machine learning pipelines while collaborating with cross-functional teams to translate quantitative findings into actionable insights.
The Associate Director will provide statistical leadership and support for clinical trials within a pharmaceutical client's global therapeutic group. Responsibilities include developing clinical trial protocols, overseeing vendor deliverables, and utilizing advanced statistical methods and machine learning to derive actionable insights.
The Director of Business Development is responsible for driving revenue growth and managing customer relationships within the DACH territory. They will act as a trusted advisor to clients, evangelizing the company's vision and implementing effective go-to-market strategies.
The role involves supporting the Epidemiology team by preparing Real World data and conducting statistical analysis to inform clinical development and safety documents. You will also partner with stakeholders to manage projects and provide technical expertise for observational studies.
The Associate Director provides senior technical leadership and functional guidance for epidemiological programming, ensuring high-quality, reproducible outputs for real-world evidence studies. They also manage programming strategies, mentor team members, and collaborate with cross-functional partners to support complex research objectives.
You will support the epidemiology team by preparing real-world data, conducting statistical analyses, and developing innovative methods for data standardization and reporting. The role involves partnering with internal and external stakeholders to manage projects and ensure the timely delivery of high-quality analytical insights.
The Principal Statistical Programmer will work independently to implement reporting and analysis activities for sponsor clinical trials. They will also oversee CRO programmers to ensure consistent, high-quality data summaries across various therapeutic areas.
The role involves leveraging advanced SAS programming and CDISC standards to support or lead Phase I-IV clinical trials for a global pharmaceutical client. Responsibilities include data manipulation, analysis, and reporting within a globally dispersed team environment.
The Senior Statistical Programmer will lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. They will be embedded within a pharmaceutical client to drive innovation in patient treatment through data analysis and reporting.
Lead Phase I-IV clinical studies and provide statistical expertise for clinical development plans, protocols, and concept sheets. Formulate integrated analytical approaches using statistical methods and machine learning to discover actionable insights and automate processes.
The Principal Statistical Programmer implements reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They are also responsible for overseeing CRO programmers to ensure high-quality and consistent data summaries.
