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Manage and ensure compliance of study documentation, support TMF processes, conduct quality reviews, and assist in audits and training tasks.

Lead the planning, execution, and delivery of Phase I global clinical trials, ensuring adherence to timelines and performance metrics while collaborating with cross-functional teams.

The Sr. TMF Specialist is responsible for processing study documents, ensuring compliance, conducting reviews, and supporting TMF activities throughout the study lifecycle.

The VP of Corporate Products leads the technology organization supporting corporate functions, overseeing AI implementation and product management, ensuring efficient tech operations and strategic alignment with business objectives.

The Lab Equipment Specialist I provides laboratory support, including maintenance, troubleshooting, reagent preparation, and packaging waste in a regulated environment.

The Analytical Scientist II performs sample processing, develops bioanalytical methods, documents analysis activities, and verifies data as part of regulatory compliance.

The Sr Clinical Trial Manager oversees site management, ensures regulatory compliance, coordinates project deliverables, and mentors Clinical Trial Managers for successful project execution.

The Sub-Investigator supports the Medical Director in clinical trial management and participant care, ensuring protocol adherence and effective communication during studies.

The Senior Information Security Governance Analyst manages the cybersecurity governance framework, develops policies, leads initiatives, conducts audits, and promotes awareness, ensuring compliance with regulations and industry standards.

Manage clinical trial agreements, develop site budgets, negotiate contract terms, and ensure compliance with regulations while maintaining stakeholder relationships.