Medical Monitor
Medical Monitors provide medical input to global clinical studies with patient safety focus; home-based in Canada.
Remote • Canada- Full Time
- Min. 10 YOE
PSI CRO AG
115 open rolesLast updated May 5, 2026 at 8:31 AM UTC
All open jobs at PSI CRO AG
Browse the full live job inventory for PSI CRO AG. This page is focused on current openings, while the overview tab highlights role groups and hiring patterns.
115 open positions
Designer
Designer shapes visuals for clinical trial documents, ensuring brand consistency across departments.
Hybrid • Warsaw, Poland- Full Time
- Min. 3 YOE
Designer
Design-focused role creating and maintaining client-facing visuals, with global collaboration and brand consistency.
Hybrid • Budapest, Hungary- Full Time
- Min. 3 YOE
Administrative Assistant Data Management
Administrative assistant role supporting departmental calendars, training plans, and document management in Budapest.
- Hybrid • Budapest, Hungary
- Full Time
- Min. 3 YOE
Site Technology Specialist
Provide technical support and expertise on technology to clinical sites, coordinating study-related technologies and training.
Remote • United States- Full Time
- Min. 5 YOE
Referral Network Specialist
Builds and manages a country-specific network of referring physicians to support PSI CRO's referral programs.
On-site • Saint-Maur-des-Fossés, France- Full Time
- Min. 3 YOE
Clinical Trials Lead Site Coordinator
Coordinate trial site activities, ensure enrollment goals, and support regulatory/documentation processes.
On-site • Mexico City, CDMX, Mexico- Full Time
- Min. 2 YOE
Grants Expense Coordinator
Coordinate grant budgets and payments across international clinical projects, ensuring accurate reimbursements and timely settlements.
- Full Time
- Min. 2 YOE
Clinical Research Associate II / Senior CRA
Monitor onsite visits, study startup, source verification, and site communication across diverse therapeutic studies.
On-site • Tbilisi, Georgia- Full Time
Site Management Associate (Clinical Trials)
Coordinate site communications and document management for clinical research projects in Tbilisi with focus on communication, databases, and meeting coordination.
- On-site • Tbilisi, Georgia
- Full Time
IT Compliance Specialist
Support IT governance by creating, updating, and processing internal IT documents for audits and compliance.
Hybrid • Utrecht, Netherlands- Full Time
IT Compliance Specialist
Ensure IT compliance through documentation, audits, and risk assessments for in-house systems.
Remote • Latvia- Full Time
- Min. 2 YOE
Principal Statistician
Leads statistical analysis and project coordination for global clinical trials with SAS and CDISC ADaM expertise.
Remote • United Kingdom- Full Time
Lead Clinical Research Associate
Lead project teams in site monitoring, CAPA, audits, and data integrity across country/region.
- Remote • Canada
- Full Time
- Min. 4 YOE
Principal Statistician
Lead statistical activities for global clinical trials, coordinating with international statisticians, programmers and data managers.
- Remote • United States
- Full Time
- Min. 5 YOE
Site Identification Specialist
Maintain and refine internal site database; develop site identification strategies and due diligence for investigators and sites.
On-site • Shanghai, China- Full Time
- Min. 2 YOE
Regulatory Officer
Regulatory liaison and dossier preparation for clinical trials, ensuring submissions and regulatory compliance across PSI countries.
- Full Time
- Min. 5 YOE
Clinical Trial Liaison
Coordinate site-specific patient recruitment and retention plans observing planned metrics and provide enrollment progress analysis to improve patient pathways.
- On-site • Budapest, Hungary
- Full Time
- Min. 5 YOE
Regional Project Lead
Coordinate project teams in Japan to meet study milestones and report progress to clients and global stakeholders.
Remote • Japan- Full Time
- Min. 4 YOE
Principal Statistician
Oversees statistical activities for global clinical trials, leading SAS programmers and statisticians in CDISC ADaM, interim/final analyses, and audits.
- Remote • France
- Full Time
- Min. 5 YOE
Regulatory Officer
Prepare regulatory submission dossiers and liaise with authorities to support clinical trials in Japan.
- On-site • Tokyo, Japan
- Full Time
- Min. 1 YOE
Regulatory Officer (Clinical Trial Submissions)
Regulatory submissions coordination for clinical trials in Kazakhstan, preparing dossiers and liaising with authorities.
On-site • Almaty, Kazakhstan- Full Time
- Min. 1 YOE
Coordinator, Regional F&A (OOP Compiling)
Coordinate OOP expense reconciliation and reporting across the region with cross-functional collaboration.
Hybrid • Sofia, Bulgaria- Full Time
- Min. 5 YOE
Junior IT Systems Administrator
Provide daily technical support for IT systems, troubleshooting desktop issues and coordinating IT requests.
On-site • Buenos Aires, Argentina- Full Time
- Min. 1 YOE
Scroll for more jobs