
1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
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1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.
• Streamline activities of project teams and ensure consistency of Clinical Operations processes across the Asia Pacific region • Ensure study milestones are met by project teams at country level • Report study progress to clients and global stakeholders • Act as project management contact for the project team and PSI support services • Perform study status reviews and progress reporting; collect and report project status updates • Develop and update project planning documents, essential study documents, and project manuals/instructions • Ensure project timelines and subject enrollment targets are met • Coordinate maintenance of study-specific and corporate tracking systems • Oversee site selection and startup, and site contractual and budget negotiations • Supervise project team and site training; perform field training of monitors tailored to project needs • Ensure team compliance with the project-specific training matrix • Supervise preparation, conduct, and reporting of site selection, site initiation, routine monitoring, and closeout visits • Review site visit reports and ensure monitoring and reporting standards are met • Oversee investigator and site payments • Supervise project team preparation for study audits/inspections and resolution of audit/inspection findings • Participate in regional project oversight for APAC as needed
• MPharm, RN or university/college degree in Life Sciences, or an equivalent combination of education, training and experience • Minimum 4 years’ site monitoring experience • At least 2 years’ experience as Lead Monitor, preferably in regional capacity • Experience supervising clinical project activities and leading clinical project teams • Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable • Communication, presentation, and customer-service skills • Team building, leadership, and organizational skills • Full working proficiency in English • Proficiency in MS Office applications, including MS Project
• Stable and secure workplace • Professional development and investment in employees’ success • Inclusive culture where colleagues feel welcomed and valued • Remote work option
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