Clinical Regional Project Lead

PSI CRO·Shanghai, Shanghai, China

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About the role

On-site, full-time regional clinical project leadership role in Shanghai, managing China-based project teams, timelines, milestones, reporting, process consistency, vendors and study systems. Requires at least 8 years of site monitoring experience in China and at least 2 years as a Lead Monitor, plus a specified pharmacy, nursing, life sciences, or equivalent education route. Full working proficiency in English and Chinese is required.

Key requirements

• MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience
• At least 8 years of relevant experience
• Required skills: Site monitoring in China, Supervision of clinical project activities, Leading clinical project teams, Clinical project timeline, milestone and schedule management, Project status reporting, Regional clinical operations process consistency, Communication with global project managers and clients, Team building, Leadership, Organizational skills, Quality compliance, Training, Vendor and contractor coordination, Clinical project planning documentation, Study tracking systems, Full working proficiency in English and Chinese, MS Office applications, MS Project
• Required languages: English, Chinese

Opportunity details

• Workplace: On Site
• Posted: Nov 13, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Clinical Regional Project Lead

Location: Shanghai, Shanghai, China

Employment type: Full-time

Company Description

PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

In this role you will streamline activities of project teams in China and ensure consistency of Clinical Operations processes across regions. You will ensure meeting study milestones by project teams on a country level, report study progress to clients and global stakeholders.

The scope of responsibilities will include:

Manage clinical project timelines, milestones, schedules and updates during all project stages
Report project status updates and progress for a designated region; participate in Projects Review Meetings
Ensures consistency of all study processes across regions and identify regional differences
Communicate with Global Project Managers and clients
Manage project teams in the region, including team building, quality compliance, training and and monitoring of daily activities
Be a point of contact for contractors and third party vendors
Contribute to the development and update of project planning documents, essential documents, and project instructions
Oversee maintenance of study-specific and corporate tracking systems
Might be involved in regional project oversight for APAC

Qualifications

MPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experience
Minimum 8 years’ site monitoring experience in China
At least 2 years’ experience as Lead Monitor
Experience supervising clinical project activities and leading clinical project teams
Experience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferable
Communication, presentation, and customer-service skills
Team building, leadership and organizational skills
Full working proficiency in English and Chinese
Proficiency in MS Office applications, including MS Project