PSI CRO AG
Healthcare Insurance • Pharmaceuticals • Science
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.
Clinical Research Associate II
July 31
🗣️🇪🇸 Spanish Required
PSI CRO AG
Healthcare Insurance • Pharmaceuticals • Science
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 all types of onsite monitoring visits • Be involved in study startup and feasibility research • Perform CRF review, source document verification and query resolution • Be responsible for site communication and management • Be a point of contact for in-house support services and vendors • Communicate with internal project teams regarding study progress • Support regulatory team in preparing documents for study submissions
🎯 Requirements
• College/University degree in Life Sciences or an equivalent combination of education, training & experience • 1 - 2 years of independent on-site monitoring experience in Mexico • Experience in all types of monitoring visits in Phase II / III • Full working proficiency in English and Spanish • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel
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