Lead the finance business partnering team, oversee project finances, ensure timely reporting, develop financial forecasts, and drive process improvements.

The Regulatory Scientist will support regulatory submissions for clinical trials, ensure compliance with regulations, and manage documentation systems while collaborating with internal stakeholders.

As an Ops Support Analyst I, you will provide support for IRT systems in clinical trials, assist in troubleshooting, monitor system performance, collaborate with teams, and maintain documentation.

The Senior Statistical Programmer is responsible for designing and validating SAS programs for clinical trial data analysis, mentoring junior staff, and ensuring regulatory compliance.

The Business Analyst I will analyze performance, develop tracking tools, conduct cost/benefit analyses, collaborate across departments, and manage KPIs.

The Clinical Database Programmer designs and manages clinical databases for trials, ensuring operational excellence and compliance with quality standards.

As an Investigator Payment Associate, you will process investigator payments, maintain compliance documentation, resolve discrepancies, and assist in financial reporting.

The Accounts Receivable Associate will manage invoicing, ensure compliance with contracts, collaborate on audits, and maintain client relationships to facilitate smooth financial processes.

Manage vendor data accuracy and compliance in the masterfile system, support procurement processes, and perform data analysis for improvements.

The Senior Manager of Financial Business Partnering will provide strategic financial insights, lead financial analysis, and mentor financial analysts to enhance business performance.

The Site Specialist II supports start-up activities for clinical trial sites, manages contracts, and ensures compliance through effective collaboration and communication.

As a Financial Analyst II, you will support financial planning and analysis, develop financial models, prepare reports, and identify process improvements.

Lead the Project Finance & Analysis team, ensuring accuracy in financial reports, managing budgets, and providing insights to support decision-making. Foster team development and maintain relationships with project managers to track financial performance effectively.

The Accounts Receivable Associate will manage invoicing, ensure compliance with contracts, collaborate with Project Managers, and support month-end processes.

The Senior Validation QC Analyst will lead clinical data validation processes, ensuring compliance and data integrity while mentoring junior analysts and collaborating with various teams.

Develop and validate statistical programming code for clinical trial data analysis and reporting, ensuring data integrity and compliance with standards.

The Director of Site Activation will lead centralized clinical study operations, manage high-performing teams, drive process improvements, and implement strategies for transformation and efficiency.

The Financial Accountant II will manage financial transactions, prepare financial statements, ensure accounting compliance, and support budget preparation.

The eCOA Screen Review Associate reviews eCOA screenshots, tests applications for usability, manages projects, communicates with clients, and conducts data analysis to support clinical research efforts.

The Data Quality Analyst will track, report, and analyze operational metrics to ensure high standards in clinical development, communicate insights to stakeholders, and validate data quality.