PSI CRO AG
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.
Site Management Associate I
đ„ 2 minutes ago
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PSI CRO AG
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 Description
âą Be the main point of contact between site personnel and CRA involved in the project âą Assists the Monitors in their prompt completion of all subject event and site event information in CTMS âą Ensure that pre-study testing of local site facilities is completed âą Track the resolution status of site issues and action items in CTMS âą Act as the one who ensures the order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies âą Ensures regulatory and ethics committee submissions and notifications âą Manage the TMF on a site and a country level for regularly and file documents âą Prepare, distribute, and update Investigator Site Files (ISF) and ISF checklists âą Document Management and translations status review of the study
đŻ Requirements
âą College/University Degree in Life Sciences âą Administrative work experience, preferably in an international settings âą Prior experience working as CTA for CROs âą Prior experience working in Clinical Research âą Local regulations knowledge âą Full working proficiency in English âą Proficiency in MS Office applications âą Ability to plan and work in a dynamic team environment âą Communication and collaboration skills
đïž Benefits
âą Remote work options
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