We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
You will join a global yet closely-knit team with a shared commitment to developing smart and effective approaches to project monitoring. You will have the opportunity to help shape the future of risk-based monitoring at PSI and contribute to ensuring high-quality study data. As part of your role, you will remotely monitor study data, identify potential errors and trends, and flag issues related to site performance.
Hybrid position after trial period.
You will:
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
Support clinical research projects by managing communication, documentation, and regulatory compliance while serving as the main contact for site personnel and vendors.
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