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Manage and govern executive and equity compensation programs, including analysis, modeling, grant lifecycle administration, compliance (SOX, tax, Section 16), stakeholder communications, vendor management (Fidelity), reporting to leadership and the Board, and process improvements across jurisdictions.

Assist in implementing and supporting safety systems, conduct configurations, data extraction, user training, and ensure compliance with safety regulations.

Oversee site management for clinical studies, conduct monitoring visits, ensure compliance with regulatory standards, safeguard data integrity, manage project plans, and facilitate training, maintaining quality control throughout clinical trials.

Oversee start-up phase of clinical trials, ensuring regulatory compliance, site management, and strong communication between sponsors and sites. Manage essential documents and site activation requirements.

As a Senior Statistical Programmer, you will develop and validate SAS programs for clinical trial data analyses, support regulatory submissions, and lead studies, impacting patient health globally.

As a Principal Statistical Programmer, oversee programming activities on clinical studies, mentor team members, and ensure quality outputs while interacting with cross-functional teams.

The Senior CRA will conduct national monitoring for various therapeutic areas, focusing on oncology and other specializations, while working with multiple protocols.

Manage and monitor clinical studies, ensuring compliance with regulatory requirements and protocols while maintaining data integrity and safety of participants.

Responsible for monitoring clinical studies, ensuring compliance with regulatory requirements, data integrity, and support for study teams in oncology projects.

The Director, Global Strategic Sourcing will lead strategic sourcing and category management, managing a global team, ensuring alignment with business priorities, and delivering value through effective sourcing strategies and stakeholder engagement.