PSI CRO AG
1001 - 5000 employees
Founded 1996
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🔬 Science
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.
Senior Clinical Research Associate
🕒 April 14
🗣️🇪🇸 Spanish Required
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PSI CRO AG
1001 - 5000 employees
Founded 1996
⚕️ Healthcare Insurance
💊 Pharmaceuticals
🔬 Science
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
• Train and coordinate junior CRAs on site • Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits • Deliver training to investigators, site staff, and project teams • Work with complex studies • Perform CRF review, source document verification, and query resolution • Manage site communication and management • Be involved in site identification process • Contact for clinical investigators, vendors, and support services regarding study progress • Participate in feasibility research • Prepare and deliver presentations at Investigator’s Meetings • Prepare for and attend company audits; resolve audit findings • Support Regulatory Affairs in procuring site regulatory documents • Maintain study-specific automated tracking systems
🎯 Requirements
• College/University degree in Life Sciences or equivalent • Full working proficiency in Spanish and English • At least 3 years of 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 (a plus) • Proficiency in MS Office applications
🏖️ Benefits
• Professional development • Tailored courses and mentoring • Health insurance (implied) • Paid time off (implied)
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