
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„ 0 minutes ago
đ§đ· Brazil â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
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 0 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 Conduct and report all types of onsite monitoring visits âą Be involved in study startup and feasibility research âą Perform CRF review, source document verification and query resolution âą Be responsible for site communication and management âą Be a point of contact for in-house support services and vendors âą Communicate with internal project teams regarding study progress âą Support regulatory team in preparing documents for study submissions
âą College/University degree in Life Sciences or an equivalent combination of education, training & experience âą Independent on-site monitoring experience âą Experience in all types of monitoring visits in Phase II / III âą Experience in Oncology is preferred âą Full working proficiency in English and Spanish 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 Ability to travel
âą Opportunity to further develop skills âą Opportunity to widen therapeutic area experience âą Opportunity to become an expert in clinical research
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