In this role you will streamline activities of project teams and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.
The scope of responsibilities will include:
- Act as project management contact for the project team and PSI support services.
- Perform study status review and progress reporting, collect and report project status updates.
- Develop and update project planning documents, essential study documents and project manuals/ instructions.
- Ensure that the project timelines and subject enrollment targets are met.
- Coordinate maintenance of study-specific and corporate tracking systems.
- Oversee site selection and startup, site contractual and budget negotiations.
- Supervise project team and site training, perform field training of monitors tailored to the project needs.
- Ensure team compliance with project-specific training matrix.
- Supervise preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits.
- Review site visit reports and ensures monitoring and reporting standards are met.
- Oversee investigator and site payments.
- Supervise project team preparation for study audits/ inspections and resolution of audit/ inspection findings.
- Might be involved in regional project oversight for APAC.
Apply on company website Singapore Hybrid Full-time
PSI CRO is hiring a Clinical Regional Project Lead
About company
PSI is a leading full-service global Contract Research Organization (CRO). The company specializes in delivering pivotal Phase 2 and Phase 3 clinical trials on time and on budget, with predictable patient enrollment across multiple therapeutic areas.
PSI focuses on a wide range of therapeutic areas including Oncology, Gastroenterology (GI), Hematology, Cell and Gene Therapy, Neurology, Infectious Diseases, Radiopharmaceuticals, and Respiratory diseases, among others.
The company leverages advanced platforms like Visional for clinical trial feasibility analysis and Synetic for site intelligence and study acceleration, aiming to protect trials from delays and budget overruns through data-driven solutions.