Jobs at PSI CRO

Leads clinical trial delivery across designated countries, coordinating project teams, timelines, enrollment, budgets, site activities, regulatory submissions, monitoring, training, quality, audits, and performance reporting. Partners with Project Managers, sponsors, CRAs, investigators, and cross-functional teams while supervising regional staff and resolving resourcing or performance issues. Requires clinical research and independent monitoring experience, Clinical Trial Manager or Study Manager experience, and therapeutic expertise in Oncology or Gastroenterology.

Supports clinical research projects by coordinating communication with investigative sites and vendors, managing clinical supplies and payments, facilitating regulatory and ethics submissions, maintaining Trial Master Files and Investigator Site Files, tracking study information, supporting audits and meetings, and ensuring safety information flows appropriately. The role is office-based in Banja Luka and requires medical or pharmacy education, strong organization, multilingual communication, and Microsoft Office proficiency.

Supports clinical research sites by coordinating communication between site personnel, CRAs, vendors, and study teams. Responsibilities include resolving queries, maintaining CTMS, managing clinical supplies and site files, coordinating regulatory submissions, supporting audits and inspections, tracking training and document status, and ensuring safety information flows properly. The role requires clinical research knowledge, familiarity with local regulations, strong administrative and communication skills, English proficiency, and Microsoft Office experience.

Supports clinical research projects by coordinating communication with investigative sites and vendors, managing clinical supplies and payments, maintaining Trial Master Files and Investigator Site Files, tracking study systems, supporting regulatory and ethics submissions, coordinating audits and meetings, and ensuring safety information flows appropriately.

Supports clinical research projects by maintaining databases, tracking systems, and documents; coordinating communication with investigative sites; resolving queries; arranging meetings; supporting training and system access; and handling correspondence. The role requires strong organization, multitasking, problem-solving, Polish and English fluency, Microsoft Office proficiency, and a life sciences degree.

Manage clinical project finances for a contract research organization, including study and change-order budgets, financial analysis, accrual reporting, invoicing requests, sponsor contracts, payment schedules, and timesheet reconciliation. The role supports proposals and contract management while maintaining project finance data, ensuring accurate reporting, coordinating with departments and sponsors, and training colleagues.

Manage end-to-end recruitment across China, partnering with hiring managers, sourcing and assessing candidates, coordinating interviews, building talent pipelines, and maintaining positive candidate experiences. The role also manages recruitment agencies, ATS data, reporting, sourcing-channel evaluation, and continuous recruiting improvements. It requires bilingual Mandarin and English communication and may support hard-to-fill technical, R&D, and clinical research positions.

Manage day-to-day accounting for the Argentine legal entity, including SAP data maintenance, reporting, month-end close support, documentation, and coordination with external accounting and tax providers. Coordinate selected accounting processes across LATAM, especially Brazil and Mexico, by monitoring data quality, following up on outstanding information, clarifying accounting questions, and supporting consolidated group reporting. The role requires independent work, attention to detail, strong communication, and fluent English.

Manages financial activities for clinical research projects, including study budget development, budget maintenance, accrual reporting, invoicing, sponsor contracts, payment schedules, and timesheet reconciliation. Supports proposals and contract management while analyzing actual versus budgeted costs. The role requires clinical trial budgeting experience within a CRO, advanced Excel skills, strong analytical and communication abilities, and the capacity to coordinate with sponsors and internal departments.

Manage clinical project finances for a contract research organization, including study budget development, change orders, sponsor contracts, payment schedules, accrual reporting, invoicing, timesheet systems, and budget-versus-actual reconciliation. The role supports proposals and contract management while coordinating with internal departments and sponsors. It also requires accurate reporting, negotiation, organization, multitasking, and training colleagues.

Manage clinical study budgets, change orders, sponsor contracts, payment schedules, accruals, invoices, and project-specific timesheets. Analyze actual versus budgeted costs, prepare forecasts and finance reports, maintain project finance data, support proposals and contract management, and negotiate budgets within global CRO and pharmaceutical projects.

Manage clinical trial project finances, including study budgets, change orders, sponsor contracts, payment schedules, accrual reports, invoicing requests, and timesheet reconciliation. Maintain project finance data in internal systems, analyze actual versus budgeted costs, support proposals and contract management, and coordinate with sponsors and internal departments. The role also requires accurate reporting, negotiation, organization, multitasking, and training colleagues.

Manage clinical study budgets from proposal development through project completion, including change orders, forecasts, accruals, invoicing requests, sponsor contracts, payment schedules, and actual-versus-budget reconciliation. Maintain project finance data and timesheet systems, support contract management, analyze budgets, and provide accurate financial reporting. The role also requires budget negotiation, scope management, communication, organization, and training capabilities within a clinical research environment.

Manage clinical project finances for a contract research organization, including study and change-order budgets, financial system setup, accrual reporting, invoicing requests, sponsor contracts, payment schedules, and timesheet reconciliation. The role requires financial analysis, budget management, sponsor negotiation, cross-functional communication, accurate reporting, and training support in a hybrid Buenos Aires setting.

Manages clinical project finances for a contract research organization, including study and change-order budgets, financial analysis, accrual reporting, invoicing requests, sponsor contracts, payment schedules, and timesheet reconciliation. Supports proposals and contract management while maintaining project finance data, ensuring accurate reporting, coordinating with sponsors and internal departments, and training others.

Manage financial activities for clinical research projects, including study budgets, change orders, sponsor contracts, payment schedules, accrual reports, invoicing requests, and timesheet reconciliation. The role supports proposals and contract management while maintaining accurate project finance data, analyzing budget versus actual costs, communicating with sponsors and internal departments, and training colleagues.

Provides strategic and operational HR support during a 12-month maternity cover. Responsibilities include employment formalities, benefits, HR policy and records administration, attendance and performance processes, training coordination, recruitment support, payroll verification, employee relations, compliance, and stakeholder advising across local and global teams.

Supports clinical trial site operations by managing site communications, regulatory and ethics submissions, records, payments, audits, training, trial supplies, Investigator Site Files, and Trial Master File documentation. Coordinates query resolution, EDC completion tracking, translations, investigator meetings, and system access while providing administrative support and coaching to junior staff.

Supports clinical trial sites by managing communications, records, regulatory submissions, payments, training, trial systems, audits, Investigator Site Files, and Trial Master File activities. Coordinates site queries, EDC completion, translations, supplies, investigator meetings, and administrative issues. Provides coaching to junior staff under supervision and collaborates with monitors, vendors, investigators, and internal project teams.

Coordinates administrative and operational activities for clinical trial sites, including site communications, regulatory submissions, payments, audits, query resolution, EDC tracking, training, trial supplies, TMF and ISF maintenance, translations, and investigator meeting support. Provides coaching to junior staff and serves as a liaison among sites, monitors, vendors, and internal project teams.