PSI CRO

Global CRO delivering on-time patient enrollment

Clinical Research Associate 2/1

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeNo salary listed

About the Job

Requirements

A college or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
At least 2 years of independent on-site monitoring experience in China.
Experience conducting all types of monitoring visits in Phase II and/or Phase III studies.
Full working proficiency in English and Mandarin.
Proficiency in Microsoft Office applications.
Ability to plan and multitask in a dynamic team environment.
Communication, collaboration, and problem-solving skills.
Ability to travel up to 70% of the time.

Responsibilities

Conduct and report SSV, SIV, RMV, and COV onsite monitoring visits.
Perform case report form review, source document verification, and query resolution.
Manage site communication.
Serve as a point of contact for in-house support services and vendors.
Communicate with internal project teams regarding study progress.
Participate in feasibility research.
Support the regulatory team in preparing documents for study submissions.
Prepare for and participate in audits and inspections.

Desired Qualifications

Therapeutic area experience in Oncology is a plus.

Job Description

As a Clinical Research Associate II/I at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

You will:

Conduct and report SSV, SIV, RMV, COV onsite monitoring visits
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Be a point of contact for in-house support services and vendors
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions
Prepare and particiapte on audits and inspections

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
At least 2 years of independent on-site monitoring experience in China
Experience in all types of monitoring visits in Phase II and/or III
Therapeutic area experience in Oncology is a plus
Full working proficiency in English and Mandarin
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel, up to 70% of time

Additional Information

Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects.

Excellent working conditions
Extensive training and friendly, collegial team
Competitive salary package
Opportunities for personal and professional growth

About the Company

PSI CRO

Global CRO delivering on-time patient enrollment

PSI CRO is a global contract research organization that handles clinical trials for multiple therapeutic areas, with a focus on enrolling patients on schedule and delivering studies on time. Its services span feasibility assessments, trial planning, site selection, patient recruitment, and multi-continent trial execution across 50+ countries, backed by medical doctor resources dedicated to accurate timeline predictions. Unlike many CROs, PSI emphasizes predictable enrollment and on-time project delivery, aiming for high client satisfaction and repeat business through a pragmatic, no-nonsense approach. The company’s goal is to be regarded as the best CRO in the world by both clients and employees, achieved through reliable timelines, strong execution, and low staff turnover.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Switzerland
Founded: 1995

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