Jobs from PSI CRO

Job Description As a CRA II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is

Job Description We are seeking a highly motivated Lead Software Developer (AI) to lead the architecture, development, and implementation of AI-driven solutions supporting Data Management processes within a Clinical Research Organization (CRO). This role is ideal for a professional who can independently drive the full AI/software development lifecycle - from input into the identification of AI-auto

Job Description We are seeking a highly motivated Lead Software Developer (AI) to lead the architecture, development, and implementation of AI-driven solutions supporting Data Management processes within a Clinical Research Organization (CRO). This role is ideal for a professional who can independently drive the full AI/software development lifecycle - from input into the identification of AI-auto

Job Description This is a hybrid role with 2 days in the Oxfordshire office and 3 days working from home Full-Cycle Accounting Process all daily accounting transactions, including vendor invoices, payments, bank entries, journal postings, and intercompany transactions. Maintain accurate records across general ledger, accounts payable, accounts receivable, fixed assets, and payroll-related postings

Job Description We are now expanding Operations and looking for a dynamic and knowledgeable Coordinator to join PSI Grants Expense Management division. In this role, your goal will be to ensure that physicians and hospitals receive on time and accurate payments for their participation in the global clinical research programs. You will contribute to everything from budgets development/estimation of

Job Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Full-time permanent employment in the UK Responsibilities: Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials