PSI CRO

Senior Clinical Research Associate I

Senior Clinical Research Associate

At least 3 years’ site monitoring experience at a CRA II or equivalent qualification level in Japan, with full working proficiency in Japanese and intermediate English.

Feasibility Manager

Minimum of 5 years’ experience in clinical research and 2+ years in feasibility or patient recruitment.

Clinical Research Associate II

Clinical Research Associate

Min. 2 years of independent on-site monitoring experience in Japan, college/university degree in Life Sciences, Pharmacy, RN or equivalent.

Title	Location	Date
Senior Clinical Research Associate I Full Time · 3+ YOE Tokyo, Tokyo, Japan · Hybrid	Tokyo, Tokyo, Japan Hybrid	Aug 12, 2025
Feasibility Manager Full Time · 5+ YOE Shanghai, China · Onsite	Shanghai, China Onsite	Feb 18, 2025
Clinical Research Associate II Full Time · 2+ YOE Tokyo, Japan · Hybrid	Tokyo, Japan Hybrid	Jan 13, 2025

Activities	Clinical trial managementClinical data managementBiostatistical programmingRegulatory affairs consultingMedical writing services
Headquarters	CH
Industries	PharmaceuticalsBiotechnology
Name	PSI CRO
Employees	3,000
Type	Private
Subsidiaries	PSI Pharma Support AmericaPSI CRO UKPSI CRO GermanyPSI CRO ItalyPSI CRO France
Tagline	Manages clinical trials for the pharmaceutical and biotechnology industries.
Founded	1,995
Website	psi-cro.com

PSI CRO

About PSI CRO