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Responsible for developing sourcing strategies, performing spot buys, analyzing supplier bids, negotiating contracts, and mentoring junior staff.

Provides administrative and technical support to the Project Team, ensuring tasks are completed on time and maintaining study documentation and systems.

As a Clinical Research Associate, you will monitor compliance, manage documentation, and ensure the accuracy of clinical trials while communicating with site teams and conducting on-site visits.

As an Operations Engineer, you will support manufacturing processes, improve efficiency, collaborate across teams, and ensure quality standards for Transmission Electron Microscopes.

The Vendor Management Coordinator manages clinical supplies lifecycle, coordinates vendors, ensures compliance, and supports departmental project teams for studies.

The Site Payments Associate II provides administrative, reporting, and financial support for processing payments to investigative sites while ensuring compliance with regulations.

Provides administrative support for projects, including planning, organizing, data entry, report preparation, and quality reviews for project success.

The Director of Manufacturing Engineering leads the Engineering team, manages CAPEX planning, and develops strategies for operational excellence and compliance.

Manage the preparation, review, and negotiation of global investigator grant budgets for clinical trials, ensuring quality and accuracy while coordinating between clients and project teams.

The Sr Programmer Analyst will manage the configuration and maintenance of the Oracle Argus Safety database, developing reports and troubleshooting user queries. They will lead data migration projects and collaborate with business users on system requirements and enhancements.