PSI CRO
The Clinical Site Coordinator supports a clinical study site by managing communication between sponsors or CROs and the site, coordinating monitoring visits, tracking patient enrollment, and ensuring accurate data entry and regulatory compliance. The role also handles investigational product accountability, assists with contract and budget negotiations, and supports site payments and audit preparations.
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.
22% below the average for this role
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