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PSI CRO
The Clinical Study Coordinator supports a medical institution in clinical trial-related activities, acting as a key communication link between Milestone One, sponsors, CROs, and the site. The role involves facilitating study feasibility, managing patient recruitment and enrollment, ensuring protocol compliance, and maintaining accurate data entry in EDC systems. Additionally, the coordinator assists with regulatory documentation, training, and the handling of investigational products to ensure smooth study delivery.
PSI CRO is a full-service global Contract Research Organization (CRO) that partners with biopharma and medical device sponsors to plan and run clinical trials. The company emphasizes predictable patient enrollment across multiple therapeutic areas and offers end-to-end services such as study operations, site management, monitoring, and regulatory support. With a worldwide footprint and local operational expertise, PSI positions itself as a trusted, reliable partner for delivering clinical development programs on time.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for PSI CRO.
PSI CRO didn’t post a salary, so this is our estimate from similar listings.
36% below the average for this role
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