Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials
Overview In this role you will manage and ensure the integrity of clinical data within PSI’s global trial operations. You will collaborate with cross-functional teams to design and validate data capture, lead data quality initiatives, and support regulatory-ready databases.
Responsibilities Accountable for driving achievement of project milestones from study start‑up through to delivery of the database and monitoring of time spent on tasks. Provide Database Programming input into protocol data collection assessments. Create the annotated CRF