
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.
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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.
• Be the key support to clinical research projects • Streamline communication, maintain systems and manage documents & information • Be the main point of contact between site personnel and CRA • Assist in pre-study testing of local site facilities • Act as the one who will ensure the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies • Ensure regulatory and ethics committee submissions • Coordinate preparation for and follow-up on audits and inspections • Manage the TMF on a site and a country level
• College/University Degree in Life Sciences • Administrative work experience, preferably in an international settings • Prior experience working as CTA for CROs • Prior experience working in Clinical Research • Local regulations knowledge • Full working proficiency in English • Proficiency in MS Office applications • Ability to plan and work in a dynamic team environment
• Advance your career in clinical research • Coordinating a variety of tasks • Learning new things while growing with the company
Apply Now🕒 July 15
Site Contract Associate responsible for negotiation and execution of site contracts for clinical trials at Parexel. Contributing to a global clinical research team working remotely from Argentina, Mexico, or Brazil.
🕒 July 8
Deal Desk Associate supporting operational execution and strategic responsibilities in a global SaaS company. Contributing to order management and process improvements within a flexible and remote team.
🇦🇷 Argentina – Remote
💵 $24.6k - $55.3k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Associate
🚫👨🎓 No degree required