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The On-site Monitor will manage site activities, ensure compliance with regulations and guidelines, support data collection, and maintain communication with site staff and the project team.

The role involves leading statistical tasks in clinical studies, preparing reports, managing projects, and mentoring junior staff. It requires proficiency in SAS or R and experience in biostatistics for late phase studies.

The Clinical Trial Lead manages interdisciplinary clinical research studies, ensuring compliance with regulations, financial performance, and project deliverables while maintaining client relationships.

The Clinical Trial Manager oversees site management, ensures protocol compliance, manages risks and communication, and coordinates training and resource allocation for clinical trials.

The Executive Assistant provides high-level administrative support to the Business Unit Head, managing calendars, travel, communications, and preparing executive presentations. Skills needed include organization, discretion, and strong communication.

The Sr-Principal Biostatistician will oversee biostatistics personnel, ensure quality project outputs, prepare statistical plans, and contribute to regulatory meetings.

The Senior Proposal Analyst develops proposal budgets, prepares and modifies proposal documents, collaborates with teams, and manages the proposal process from receipt to delivery.

The Project Financial Analyst II prepares and analyzes financial reports, manages revenue recording, and supports financial planning and project evaluations for the Business Unit Controller.

The Sr Director of Operations oversees client relationships and project teams, ensuring operational excellence and strategic alignment in Real World Late Phase studies.