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

The CRA II oversees site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulations and managing site performance. Responsibilities include verifying informed consent, assessing data integrity, managing investigational products, and supporting patient recruitment, with a focus on meeting project timelines and standards.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

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 Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

Manage interdisciplinary clinical research studies, ensuring compliance, financial performance, and project deliverables while acting as a liaison with clients.

Responsible for monitoring clinical trial sites, ensuring compliance with regulatory standards, managing site activities, and supporting patient recruitment throughout study lifecycle.