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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.

Lead RWD analysis strategy and execution: develop technical specifications and statistical programs, perform complex observational analyses (propensity scoring, ML), validate cohorts/variables, ensure QC, collaborate cross-functionally, and communicate results to non-technical stakeholders.

The Senior Clinical Project Manager will lead Phase III oncology and hematology trials, managing projects and cross-functional teams while ensuring timely and quality delivery.

The Clinical Scientist contributes to protocol design, scale management, and provides training on clinical scales while ensuring data consistency and performing statistical analysis.

Provide subject-matter expertise in causal inference and construction of real-world external control arms; design protocols, analysis plans, and validation studies using RWD (claims, EHR); conduct descriptive and comparative analyses; communicate methods and results in regulatory documents, reports and publications; manage stakeholders and vendors; and contribute to process and training improvements to support RWE strategy execution.

Lead biostatistics activities for clinical and laboratory data using R, JMP, and SAS. Mentor statisticians, prepare SAPs, verify analyses, produce regulatory-ready tables/figures, perform data integration and QC, support DSMBs, and contribute to proposals and regulatory interactions.