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Lead site monitoring activities for global clinical trials, ensuring compliance with safety, data integrity, and regulatory standards while overseeing trial management and fostering interdepartmental collaboration.

The role involves budgeting for clinical trials, negotiating contracts, collaborating with sponsors, ensuring compliance, and training junior staff.

The Clinical Data Reviewer will work in the oncology field, ensuring data integrity for clinical trials and collaborating with teams to meet customer needs.

The CST Project Manager oversees Clinical Surveillance & Training projects, ensuring quality delivery, managing vendor relationships, and maintaining project documentation.

The Principal Clinical Data Scientist leads clinical data management for complex studies, ensuring data quality, compliance, and timely delivery of milestones while collaborating across teams to address data-related issues and support analytics innovation.

Lead feasibility strategy for clinical programs, assess trial locations, engage stakeholders, analyze data, and prepare reports to ensure successful trial execution.

The Senior Site Contracts Manager negotiates and manages US site budgets and clinical trial agreements, collaborating with various stakeholders to ensure compliance and support operational excellence.

The Site Contracts Manager will negotiate and manage US site budgets and clinical trial agreements, ensuring operational excellence and compliance while collaborating with stakeholders.

Manage biomarker studies and oversee biomarker operations in clinical trials, ensuring high standards in sample collection and analysis. Lead cross-functional teams through the trial lifecycle while managing project timelines, budgets, and quality.

Manage and negotiate site contracts and budgets for industry-sponsored clinical trials, coordinate with legal/finance/operations, ensure contract execution and archival, mentor junior staff, track milestones, and maintain SOP/WI compliance.