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
Clinical Research Associate
April 30
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
• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits • Delivering training of investigators, site staff and project teams • Work with complex studies • Perform CRF review, source document verification and query resolution • Be responsible for site communication and management • Be involved in site identification process • Contact for clinical investigators, vendors and support services in regard to study progress • Participate in feasibility research • Preparation and delivering of presentations at Investigator’s Meetings • Preparation for and attendance at company’s audits; resolution of audit findings • Support to Regulatory Affairs in procurement of site regulatory documents • Maintenance of study-specific automated tracking systems
🎯 Requirements
• Bachelor's degree in Medicine • At least 2 years experience in patient care and/or health care or clinical environment • Full working proficiency in Spanish and English • Experience in Clinical Research is a plus • Availability to travel • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment • Communication, collaboration, and problem-solving skills
🏖️ Benefits
• A dynamic, global company founded in 1995 • Committed to develop our employees in their careers by providing tailored courses and mentoring • Opportunity to develop yourself as a senior, trainer, mentor and leader
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