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As an Associate Legal Counsel, you will provide legal support focused on local matters in Ukraine, including reviewing and drafting contracts, providing legal advice, and ensuring compliance with company policies. You will collaborate closely with various departments and assist in legal matters related to clinical trials.

As a Budget Specialist, you will support clinical research projects by reviewing and negotiating site budgets, facilitating agreements, and maintaining documentation. You'll work with various teams to ensure contracts are executed and tracked, contributing to the efficient functioning of clinical trials.

As a Full Stack Developer at PSI, you will develop and maintain business applications, process user requests, prepare documentation, implement software tests, and track development tasks. You will also remain updated on systems development technologies.

As a Full Stack Developer, you'll architect, develop, and maintain business applications, support internal IT system requests, document development processes, conduct code reviews and testing, and adhere to development standards. The position requires collaboration and staying updated with technological advancements.

The Site Management Associate I supports clinical research projects by managing communication, documents, and site-related tasks. Responsibilities include query resolution, ensuring compliance with local regulations, coordinating audits, and managing supplies and training for site teams.

As a Site Management Associate I, you will support clinical research projects by managing communications, maintaining systems, handling document management, and ensuring compliance with regulations. You will act as a liaison for site personnel and oversee the inventory of clinical supplies, regulatory submissions, and training for project teams, facilitating efficient project execution.

The Site Management Associate I will support clinical research projects by managing communication, coordinating site activities, and handling documents while ensuring compliance with regulatory standards. Responsibilities include acting as a liaison between site personnel and clinical research associates, managing supplies, tracking regulatory submissions, and overseeing audit preparations.