
1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • 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.
🕒 October 20
Where this job comes from
Posted on PSI CRO AG's careers page, not through a job board
First seen by Remote Rocketship October 20
Still open on PSI CRO AG's site. Checked Yesterday.

1001 - 5000 employees
Founded 1996
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • 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.
• Facilitate negotiations of site agreements and budgets to align with the site activation plan • Customize and prepare country- and site-specific agreements and organize translations • Track the status of site agreement and budget negotiations • Prepare executable versions of site agreements and budgets and coordinate the signature process • File executed site agreements in the Trial Master File • Update all concerned functions on the site contracting process
• College or university degree or an equivalent combination of education, training, and experience • Equivalency requires a minimum of 2 years’ experience in an environment where relevant experience has been gained • Minimum 2 years’ experience in the clinical research industry • Previous experience negotiating site budgets • Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus • Must not require a work visa for employment or continued employment now or anytime in the future • Based anywhere in the United States
• Employees can work remotely • Opportunity to work for a dynamic, global company focused on medical science and bringing new medicines to patients • People-focused company culture
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