
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 6 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 6 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 management ⢠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 ⢠Build strong site relationships across Germany nationwide and, where applicable, Switzerland ⢠Make decisions, solve problems, and drive study success ⢠Work across multiple sponsors, broad therapeutic areas, and complex clinical trials
⢠College/University degree in Life Sciences or an equivalent combination of education, training & experience ⢠Independent on-site monitoring experience in Germany ⢠Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III ⢠Experience in Switzerland is a plus ⢠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 ⢠Valid driverâs license
⢠Competitive salary and comprehensive benefits package ⢠Excellent and flexible working conditions supporting work-life balance ⢠Structured onboarding with hands-on mentoring ⢠Continuous mentoring ⢠Clear career development opportunities and visible internal growth paths ⢠Stable environment where long tenures are common and career building is encouraged ⢠Supportive managers and approachable leadership ⢠Technologically integrated environment with in-house systems designed to reduce administrative burden ⢠Autonomy and trust in decision-making ⢠Collaborative culture and knowledge sharing across borders
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