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Lead and manage the HR Shared Services team to ensure efficient delivery of HR services and maintain compliance with policies.

Perform activities in clinical operations, assist with site management, maintain project files, ensure compliance, and coordinate team meetings. May provide mentorship.

The role involves monitoring clinical trials, ensuring compliance with regulations, managing site activities, and collaborating with site staff, requiring oncology experience and strong communication skills.

Oversee Phase 1 clinical research studies, ensuring adherence to protocols and timelines, while collaborating with stakeholders and supervising support staff.

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.