- Conduct and report all types of onsite monitoring visits and be involved in study startup.
- Perform CRF review, source document verification, and query resolution while managing site communication.
- Support regulatory team in preparing documents and participate in feasibility research.
PSI is a leading Contract Research Organization with 30 years in the industry, offering a balance between stability and innovation to clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.