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
15 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. • Be involved in study startup (if applicable). • 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. • Participate in feasibility research. • Support regulatory team in preparing documents for study submissions.
🎯 Requirements
• College/University degree in Life Sciences or an equivalent combination of education, training & experience. • Independent on-site monitoring experience in Mexico. • Experience in all types of monitoring visits in Phase II and/or III. • Availability to travel. • Experience in Oncology or Infectious Diseases is a plus. • Full working proficiency in English and Spanish. • PC skills to be able to work with MS Word, Excel and PowerPoint. • Ability to plan, deal with different tasks and work in a dynamic team environment. • Communication, collaboration, and problem-solving skills.
🏖️ Benefits
• Become a full-fledged clinical research professional with the support of a knowledgeable and professional team. • You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.
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