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The Sr. Site Contracts Lead oversees clinical study agreements negotiations, provides expert consultation on budgeting and contracts, trains staff, and coordinates communication among stakeholders to ensure efficient contract execution and compliance with industry standards.

The CRA II is responsible for site management activities, ensuring compliance with regulations, conducting monitoring visits, and supporting project objectives throughout the clinical trial lifecycle.

The CRA II/ SCRA performs site management tasks including qualification, initiation, monitoring, and close-out visits while ensuring compliance with regulations. They manage data integrity, assess subject safety, and engage in project communications, aiming to meet study objectives effectively.

As a Safety Specialist, you'll manage safety data, ensure compliance with regulations, perform literate screenings, and maintain safety records while enhancing team collaboration and communication.

The intern will support the Technology & Data Solutions organization by assisting in data gathering, model development, and creating visualizations, while collaborating with cross-functional teams to drive decision-making.

The Project Associate will assist in various tasks related to project management within a life sciences context, contributing to drug development and customer success.

Conduct monitoring of clinical studies, ensure compliance, develop quality monitoring tools, manage junior staff, and collaborate with cross-functional teams.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Oversee CAR-T trials in Taiwan, manage CROs, ensure adherence to study timelines, engage stakeholders, and support regulatory compliance.

The CRA performs site qualification, protocol compliance monitoring, data verification, and manages site-related activities throughout clinical trials, ensuring regulatory adherence and effective communication.