PSI CRO AG
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.
Senior Clinical Research Associate
🔥 0 minutes ago
🗣️🇫🇷 French Required
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PSI CRO AG
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.
📋 Description
• Conduct and report SIV, RMV, and COV onsite monitoring visits • Perform CRF review, source document verification, and query resolution • Manage site communication and management • Serve as a point of contact for in-house support services and vendors • Communicate with internal project teams regarding study progress • Participate in feasibility research • Support the regulatory team in preparing documents for study submissions • Prepare for and participate in audits and inspections
🎯 Requirements
• College/University degree in Life Sciences or equivalent combination of education, training, and experience • Independent on-site monitoring experience • Experience with all types of monitoring visits in Phase II and/or III • Experience in Oncology is a plus • Full working proficiency in English and French • 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 driver’s license • Must not require work visa sponsorship for employment now or in the future
🏖️ Benefits
• Remote work option • Opportunity to further develop skills • Opportunity to widen therapeutic area experience • Opportunity to become an expert in clinical research
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