
1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ 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.
đĽ 8 minutes ago
đŁď¸đŠđŞ German Required
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship 8 minutes ago

1001 - 5000 employees
Founded 1996
đĽ Healthcare
đź Consulting
đŚ 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.
⢠Conduct and report all types of onsite monitoring visits and remote visits ⢠Perform CRF review, source document verification, and query resolution ⢠Manage site communication and site relationships ⢠Participate in the site identification process ⢠Assist in training less experienced CRAs, depending on experience level ⢠Lead assigned studies, including site strategy, performance, and delivery ⢠Work across multiple sponsors and broad therapeutic areas ⢠Manage fewer protocols to enable deeper study focus and stronger site relationships across Germany nationwide and, where applicable, Switzerland
⢠College/University degree in Life Sciences or an equivalent combination of education, training & experience ⢠Independent on-site monitoring experience in Germany ⢠Experience in Switzerland is a plus ⢠Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III ⢠Experience in Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus ⢠Full professional proficiency in German and English ⢠French / Italian language skills are an asset ⢠Advanced proficiency in MS Office applications ⢠Ability to plan, multitask and work in a dynamic team environment ⢠Communication, collaboration, and problem-solving skills ⢠Ability to travel and valid driverâs license
⢠Excellent and flexible working conditions that support real work-life balance ⢠Strong culture of trust, visibility, and recognition ⢠Competitive salary and comprehensive benefits package ⢠Structured onboarding journey with hands-on mentoring ⢠Clear career development opportunities with visible internal growth paths ⢠Stable environment where long tenures are common and career building is encouraged ⢠Continuous mentoring ⢠Technologically integrated environment with in-house systems designed to reduce administrative burden
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