PSI CRO AG
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.
Number One Patient Enrollment CRO • Clinical Research • Clinical Trials • Oncology • Hematology
Senior Clinical Research Associate
17 hours ago
PSI CRO AG
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.
Number One Patient Enrollment CRO • Clinical Research • Clinical Trials • Oncology • Hematology
📋 Description
• Conduct and report all types of onsite monitoring visits as well as remote visits. • Perform CRF review, source document verification and query resolution. • Be responsible for site communication and management. • Be involved in site identification process. • Assist in training of less expert CRAs, depending on your level of experience.
🎯 Requirements
• 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 Oncology, Hematology, Infectious / Rare / Gastro-intestinal Diseases is a plus. • Full working proficiency in German, English and 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 driver’s license.
🏖️ Benefits
• Excellent and flexible working conditions. • A unique combination of team collaboration and independent work. • Competitive salary and benefits package.
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