Search the 49 jobs at PSI CRO

As a Site Management Associate I, you will ensure proper documentation exchange with sites and vendors, manage clinical supplies inventory, handle regulatory submissions, coordinate audits, and assist in training and safety management. Your role includes maintaining communication with internal teams and providing document management support.

The Site Management Associate I coordinates communication between clinical sites and vendors, manages clinical supplies, oversees regulatory submissions, handles site payments, conducts audits, supports training, and maintains document flow and tracking systems.

The Freelance Site Coordinator at Milestone One will support clinical study sites by handling communications, scheduling monitoring visits, tracking patient enrollment, maintaining study documents, and ensuring compliance with study timelines and regulatory requirements.

The Budget Specialist will support clinical research projects by reviewing and negotiating site budgets, preparing contract documents, tracking negotiation statuses in CTMS, and filing contracts. This role requires collaboration with various departments and managing documentation related to clinical trials.

The Designer will create and maintain specialized graphic materials for clinical trials, ensuring brand consistency and updating documents. Responsibilities include providing design guidance, editing materials, developing training, and conducting design training, while collaborating with global teams.

As a Full Stack Developer, you will design, develop, and maintain business applications, respond to user requests, prepare documentation, execute software tests, participate in code reviews, and track development tasks. You will ensure the quality of code and stay updated on relevant technologies.

The Site Management Associate will maintain databases, manage documents, communicate with internal and external parties, assist in meeting arrangements, and coordinate query resolutions in clinical research projects.

The Designer at PSI will create and maintain specialized graphic materials for clinical trial documents, ensure brand consistency, provide design training, and support clinical trial material design. Responsibilities include updating company documents, maintaining libraries, and editing graphics.

The Designer will create and maintain graphic materials for clinical trial documents, ensure brand consistency, maintain document templates, provide design guidance, and support training efforts while combining administrative and creative tasks.

The Designer at PSI is responsible for creating and maintaining graphic materials for clinical trial documents. This role includes ensuring brand consistency, updating templates, providing design support, and conducting training in design practices while collaborating with global teams.

The Designer at PSI will be responsible for creating and maintaining graphic materials for clinical trials, ensuring brand consistency, updating documents, and providing design support and training. The role requires collaboration with global teams and combines administrative and creative tasks in a hybrid work environment.

The Lead Data Manager oversees data management in clinical trials, ensuring effective communication with project teams and clients. Responsibilities include coordinating data management activities, developing critical study documentation, conducting user acceptance testing, and ensuring data quality and integrity. The role also involves training team members and maintaining project records.

As a Full stack Developer at PSI, you will architect, develop, and maintain business applications while supporting internal clients. Responsibilities include processing user requests, preparing documentation, executing software tests, and contributing to code reviews in a team-oriented and deadline-driven environment.

As a Full Stack Developer, you'll architect, develop, and maintain business applications. You will handle user requests for IT systems development, prepare documentation, execute software tests, and engage in code reviews while adhering to development standards and tracking tasks effectively.

The Administrator for Office Management assists with the organization and distribution of office supplies, addresses employee queries, maintains office equipment, and supports facility management tasks. Responsibilities include organizing meetings, managing courier shipments, providing information to visitors, and ensuring office security. The role demands attention to detail and good communication skills.

The Site Identification Specialist will maintain and generate relationships with investigative sites for clinical trials, manage internal databases, define study objectives, create potential site lists, and ensure compliance with regulatory standards throughout the site identification process.

The Study Startup Associate will support study startup processes by identifying and evaluating potential clinical sites, conducting site selection visits, maintaining tracking systems, and assisting with budgets, contracts, and regulatory documentation.

The Payroll Specialist is responsible for processing payroll for over 500 US and Canadian employees, administering 401K plans, assisting with audits, and ensuring compliance with various regulations. The role includes data processing for new hires and terminations, report generation, and collaboration with HR and IT teams.

As a Full Stack Developer at PSI, you'll architect and maintain business applications, process user requests, document development activities, execute software tests, and contribute to code reviews, all while advancing your professional skills in a collaborative team environment.

The SAS Programmer I will engage in statistical programming for global clinical trials, develop analysis datasets, specifications, and support program validations. Communication with international teams will be crucial for programming related to clinical research.