Search the 43 jobs at PSI CRO

Ensure on-time and accurate payments for physicians and hospitals participating in global clinical research programs. Develop payment strategies, review and approve grant budgets, and handle payment administration. Liaise with internal teams and clients for grant-related queries and maintain tracking tools for payment calculation.

Oversee and manage study startup activities in India, coordinate startup process, collect and review documents, develop site contracts and budgets, communicate with stakeholders, and facilitate cooperation between teams. Requires practical Clinical Trial startup experience in India and proficiency in English.

Fullstack .Net Developer responsible for developing in-house IT infrastructure systems, coding to support business processes, and participating in software testing and maintenance. Knowledge of C#, Microsoft .NET frameworks, React JS, HTML5, CSS, and SQL is required. Must have a BSc/BA in computer science or relevant discipline and proficiency in English.

Architect, develop, and maintain business applications, process user requests, execute software tests, follow development standards, track system development tasks, and advance professional skills.

Architect, develop, and maintain business applications. Process user requests for new development and support existing IT systems. Prepare documentation, execute software tests, follow development standards, and advance professional skills.

The Director of Quality Management will be responsible for resource management and training, quality management, quality assurance auditing, and business development. They will oversee regulatory agency inspections, management of investigations, and vendor qualification. The ideal candidate should have a minimum of 7 years of experience in clinical research and 5 years of industry experience as a QA auditor. They should have excellent knowledge of GXP guidelines, FDA/EMA regulations, and strong communication and interpersonal skills.

Part-time contract position providing technical support and expertise to clinical sites related to technology. Responsible for coordinating data collection, providing technical training, and supporting project teams with study-specific assessments.

Seeking a Software Development Project Manager with a strong background in leading teams in software, UX, and database development to build a global enterprise cloud Data Platform. Responsibilities include project development planning, team assembly, software project management, and cross-functional deliverables. Required qualifications include 6+ years of experience in managing products/services, full stack development, project management, and RDBMS administration.

The Director of Quality Management is responsible for resource management, training, quality management, quality assurance auditing, and business development in a dynamic global company focused on medical science. This role involves overseeing regulatory agency inspections, managing investigations, and developing and implementing audit plans.

Manage quality management, resource allocation, training, regulatory agency inspections, and audits. Ensure compliance with GXP guidelines and local regulations. Lead CAPA investigations and vendor qualification. Collaborate with Senior Director on staff development and research misconduct investigations.

Support a Clinical Study Site in various clinical trial related activities, maintain study documents, resolve data queries, handle investigational products, and assist in regulatory compliance.

Support Clinical Study Sites in clinical trial activities, maintain study documents, track patient enrollment, data entry, assist in monitoring visits, and facilitate regulatory compliance. Act as main communication line between Sponsor/CRO and site. Prepare for audits and inspections.

Seeking a Senior Accountant with 5 years of experience in finance and accounting to join our dynamic, global company. Responsibilities include bookkeeping, financial analysis, budget preparation, compliance assurance, payroll, and more. Full-time position based in Sofia, Bulgaria.

Reviewing, drafting, and negotiating contracts, providing legal advice and support, ensuring compliance, researching legal issues, and collaborating on clinical trial agreements and other legal matters.

The HR Specialist with focus on Payroll at PSI is responsible for ensuring timely and compliant payroll accounting, maintaining employee data, processing complex payroll issues, and supporting HR projects. They also act as a contact person for tax and social security matters and work on optimizing HR processes. Additional responsibilities include communication with authorities and providing admin support for daily operations.

The Associate Legal Counsel will be responsible for reviewing, drafting, and negotiating contracts related to clinical research, providing legal advice and support, and ensuring compliance with legal requirements. They will also support the implementation of legal policies and procedures and provide training to other departments at PSI.

The Site Coordinator supports a medical institution in clinical trial related activities, acts as communication link between Sponsor/CRO and medical institution, facilitates evaluation of proposed studies, ensures enrollment targets are met, and maintains study documentation.

The Site Coordinator supports a medical institution in clinical trial activities, facilitates communication between stakeholders, assists in data entry, monitoring visits, and ensures compliance with study protocols.

Manage local Monitors, supervise clinical monitoring activities, facilitate regional projects, train Monitors, review monitoring reports, oversee study progress, communicate with project teams, participate in quality control, and maintain tracking systems.

Manage local Monitors, supervise clinical monitoring and site management activities, facilitate regional projects, train Monitors, review monitoring reports, oversee study-specific tracking systems, and participate in quality control and compliance monitoring.