
1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
đ„ 23 minutes ago
đŁïžđȘđž Spanish Required
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship 23 minutes ago

1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
âą Train, mentor, and supervise study-level responsibilities for junior CRAs âą Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits âą Deliver training to investigators, site staff, and project teams âą Work with complex studies âą Perform CRF review, source document verification, and query resolution âą Manage site communication âą Participate in site identification and feasibility research âą Serve as contact for clinical investigators, vendors, and support services regarding study progress âą Prepare and deliver presentations at Investigator Meetings âą Prepare for and attend company audits and resolve audit findings âą Support Regulatory Affairs in procuring site regulatory documents âą Maintain study-specific automated tracking systems
âą College/University degree in Life Sciences or an equivalent combination of education, training & experience âą Full working proficiency in Spanish and English âą At least 3 years of independent on-site monitoring experience in Mexico âą Experience in all types of monitoring visits in Phase II and/or III âą Availability to travel âą Experience in Oncology or Infectious Diseases is a plus âą Proficiency in MS Office applications âą Ability to plan and work in a dynamic team environment âą Communication, collaboration, and problem-solving skills
âą Tailored courses and mentoring âą Career development opportunities âą Training, mentoring, and leadership development âą Opportunity to grow with the company
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