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.
Site Contract Specialist I
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🔥 0 minutes ago
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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
• Facilitating negotiations of site agreements and budgets to ensure alignment with the site activation plan • Customizing and preparing country- and site-specific agreements and organizing their translations • Tracking the status of site agreement and budget negotiation • Preparing executable versions of site agreements and budgets, and coordinating the signature process • Filing executed site agreements in the Trial Master File • Updating all concerned functions on the site contracting process
🎯 Requirements
• College or university degree or equivalent combination of education, training, and experience • Minimum 2 years experience in the clinical research industry • Previous experience with negotiating site budgets • Knowledge of and experience with legal documents related to clinical trial sites and medical terminology is a plus.
🏖️ Benefits
• Flexible work arrangements
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