Jobs at PSI CRO

Provide supervised desktop and peripheral troubleshooting, handle IT support tickets, assist with installation/configuration/upgrades, maintain hardware/software inventories, document issues/resolutions, and deliver basic IT training to staff.

Perform and report QA study, internal systems, location, process, and vendor qualification audits; communicate findings to project teams, operations, vendors, and clients; follow up on audit resolutions; assemble audit documentation and train operations staff on quality management.

Coordinate and streamline clinical project activities in Japan, ensure study milestones and enrollment targets are met, report progress to stakeholders, supervise project teams and monitors, oversee site selection/startup/contracts/budgets, manage KPIs, training, site visits, payments, and audit/inspection preparedness.

Provide administrative support for clinical research projects: maintain databases and tracking systems, manage documents and vendor/site communications, coordinate queries, training and access, administer site/vendor payments, handle mail/calls, assist meetings and prepare agendas/minutes.

The Central Monitoring Manager will lead risk-based monitoring implementation, oversee centralized monitoring activities, and manage communication with study teams and clients regarding patient safety and data integrity.

Responsible for full-cycle accounting, monthly and quarterly closing, group reporting, tax compliance, and annual financial statements in a hybrid role.

The Study Startup Specialist II manages clinical research study activation, maintains startup tracking systems, facilitates negotiations, supports document collection, and ensures timely project starts while communicating with project teams.

Coordinate out-of-pocket expense reporting, support financial processes, and ensure compliance while working with cross-functional teams in a regional capacity.

The Central Monitoring Manager will lead risk-based monitoring implementation in clinical studies, focusing on patient safety and data integrity, while also managing centralized monitoring activities and communicating with cross-functional teams.

The Central Monitoring Manager will lead risk-based monitoring in clinical studies, manage data integrity, present analysis results, and work with clinical teams to improve patient safety.

The Central Monitoring Manager leads risk-based monitoring implementation in clinical studies, manages data review activities, and ensures patient safety and data integrity.

Lead the implementation of risk-based monitoring, conduct centralized monitoring analysis, manage data review activities, and communicate challenges to the clinical team.

The Central Monitoring Manager will lead risk-based monitoring on clinical studies, review key risk indicators, manage centralized monitoring activities, and facilitate communication with study teams and clients.

Manage grant budgeting and payment calculations for clinical research, set up and document payment databases, coordinate with Accounting/Legal/Operations, forecast grant expenses, and report payment status to internal teams and clients.

Lead business development to recruit and onboard clinical trial sites, promote the Milestone One brand, build referral networks, manage site selection and contracting, coordinate with operations and CROs, deliver site training and performance monitoring, and ensure regulatory and contractual compliance to support trial execution and enrollment.

As a Principal Statistician, you will lead statistical activities for global clinical trials, conduct analyses, develop protocols, and guide teams of statisticians and programmers.

The Site Coordinator will support clinical trial activities, maintain communication between stakeholders, track patient enrollment, and manage regulatory documents efficiently.

Lead statistical activities in global clinical trials, performing analysis, developing protocols, and training team members while ensuring compliance with regulations.

Lead the implementation of risk-based monitoring for clinical studies, manage study risk management, and analyze data to ensure safety and integrity.

The Principal Statistician will lead statistical activities for global clinical trials, analyze data, develop statistical documents, and oversee teams while ensuring compliance with standards and regulations.