Clinical Regional Project Lead at PSI CRO

Shanghai, Shanghai, China -

Full Time

Start Date

Immediate

Expiry Date

18 Oct, 26

Salary

0.0

Posted On

20 Jul, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Project Management, Site Monitoring, Team Leadership, Quality Compliance, Vendor Management, Project Planning, Oncology, Gastroenterology, Infectious Diseases, Autoimmune Diseases, Rare Disease Indication, English Proficiency, Chinese Proficiency, MS Project, MS Office, Customer Service

Industry

Pharmaceutical Manufacturing

Description

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

Responsibilities

Streamline clinical project activities in China and ensure consistency of Clinical Operations processes across regions. Manage project timelines, milestones, and regional teams while reporting progress to global stakeholders and clients.