
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.
🔥 12 hours ago
🇮🇹 Italy – Remote
💵 €34k - €52k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
👻 Ghost score 0%
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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.
• Track database set-up, testing, maintenance and data entry • Communicate with clients, project teams and vendors on data management matters • Review study documents and design project-specific guidelines and instructions • Design eCRFs, Data Management Plans and Data Validation Plans • Test EDC databases • Ensure data entry, follow-up and validation, including manual CRF review and SAE reconciliation • Code medical data • Track and report metrics leading to database lock • Coordinate processing, dispatch and archiving of CRFs and queries • Maintain Clinical Data Management working files • Perform database QC checks • Prepare for and attend audits • Train site staff and project teams on CRF completion and data management topics
• College/University degree • Life Science or Pharmacy degree is a plus • Demonstrated experience managing clinical or medical data in a CRO is a must • Full working proficiency in English • Experience with Clinical Data Management systems (e.g. Medidata Rave, Oracle InForm) • Proficiency in MS Office applications • Organisational and time management skills • Ability to work independently and multi-task • Submit your CV in English
• Bonus • Incentive plans • Other benefits may apply • Remote work option
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