The Site Management Associate will support clinical research projects, manage documents, facilitate communication, and ensure regulatory compliance. Responsibilities include site management, document oversight, and maintaining systems for clinical trials.

The Site Coordinator supports clinical study sites by managing communication, scheduling visits, tracking enrollment, and ensuring compliance with regulatory requirements.

As a Grants Expense Coordinator, you will manage budgets, calculate payments, coordinate with teams for financial processes, and enhance payment strategies.

The Grants Expense Coordinator oversees budget planning, payment calculations, and coordination for clinical research grants, ensuring timely reimbursements and effective communication with internal teams.

The Grants Expense Coordinator manages budgets, processes payment calculations, communicates with various teams, and enhances strategies for payments in clinical research.

As a Grants Expense Coordinator, you will plan budgets, coordinate payments, communicate with teams, and enhance payment strategies for clinical research projects.

The IT Compliance Specialist will handle compliance matters for IT systems, manage documentation, support audits, and ensure adherence to standards and regulations.

The IT Systems Administrator is responsible for providing technical support, troubleshooting desktop systems, asset management, and IT training for staff.

The IT Compliance Specialist will ensure that IT systems meet compliance standards, prepare for audits, manage documentation, and assess risks.

Support clinical research projects by maintaining databases, managing documents, coordinating communications and facilitating training and meetings for site teams.

The Grants Expense Coordinator ensures timely payments for clinical trial participants, coordinates payment processes, and manages financial data for grant management tasks.

The Associate, Process Improvement will develop ontologies, collaborate with teams, conduct research, evaluate tools, and ensure data accuracy.

As an Associate, Process Improvement, you will develop and maintain ontologies, collaborate across teams, conduct research, design applications, and ensure ontology accuracy.

The Associate, Process Improvement develops and manages ontologies, collaborates with teams to improve data integration, and ensures accurate data analysis processes.

The Associate, Process Improvement will develop and maintain ontologies, collaborate with teams to improve processes, and analyze data to support knowledge management initiatives.

The AI Business Analyst will optimize AI applications, manage projects in Jira, create marketing materials, and train teams on AI tools and workflows.

The Site Identification Specialist develops strategic relationships with clinical research sites, conducts site identification activities, and collaborates with project teams to evaluate progress and resolve issues throughout clinical trials.

The Principal Statistician will lead statistical activities in global clinical trials, conduct analyses, develop protocols, and review deliverables while guiding statisticians and programmers.

The Principal Statistician will lead statistical activities for global clinical trials, oversee statistical analysis, and liaise with cross-functional teams on project-related inquiries.

The Principal Statistician leads statistical activities in global clinical trials, ensuring integrity and compliance in statistical analyses, protocols, and deliverables, while coordinating with teams and clients.