Lead and manage projects as a Senior Statistical Programmer, focusing on analysis, programming, and validating datasets with CDISC ADaM standards, while offering mentorship and support.

As an Ops Support Analyst, you will provide support for IRT systems in clinical trials, assist with troubleshooting, and ensure data accuracy.

The Financial Analyst II will analyze financial results, manage budgets, provide forecasts, and support financial performance optimization for business units.

The Senior Financial Accountant will oversee financial reporting, revenue forecasting, and support project financial analysis, ensuring accuracy and timely delivery of financial metrics and reports.

The Senior Analyst Engineer will design and optimize software solutions, collaborate with teams, and contribute to project planning while ensuring high-quality code delivery.

As a Reporting & Analytics Analyst, you will blend data from various sources to create reports, dashboards, and provide analytical support while ensuring data integrity and system configuration.

As a Statistical Programmer II, you will develop, validate, and execute statistical programs to support clinical trials, ensuring data integrity and compliance while mentoring junior programmers.

As an Epidemiologist, you will design studies, perform analyses, prepare reports, and support client engagement while ensuring compliance with policies.

The Senior Product Manager will lead end-to-end product delivery, collaborating across teams to align business needs with technology capabilities while ensuring continuous improvement and effective stakeholder engagement.

The Financial Accountant II manages financial transactions, prepares statements, ensures compliance with standards, and supports financial reporting. Key tasks include handling trial balances, VAT returns, and collaborating with auditors.

The Site Specialist II oversees clinical trial site operations including start-up, maintenance, and contract management, ensuring compliance and effective communication across teams.

The Senior Biostatistician will lead statistical analysis for clinical studies, develop analysis plans, and interpret medical data, contributing to innovative therapies.

The Senior TMF Specialist manages the Trial Master File for clinical trials, ensuring compliance with regulations, conducting checks, and collaborating with teams.

The Operation Program Specialist supports operations by managing communication, reporting, scheduling, and deliverables, ensuring timely completion and addressing bottlenecks. Responsibilities include generating reports, collaborating cross-functionally, and supporting metric development.

As an Informed Consent Specialist, you'll develop, review, and ensure compliance of informed consent forms for clinical trials, collaborating with stakeholders, managing timelines, and acting as a subject matter expert.

As a Project Manager, you'll lead global clinical trial site activations, manage study start-up planning, and ensure compliance with regulatory requirements while collaborating with stakeholders.