
200 open roles · Clinical
Clinical Regional Project Lead
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Where you can work
Unspecified
Locations named in the listing
- Shanghai, Shanghai, China
View location wording from the posting
Shanghai, Shanghai, China
Role overview
Extracted from the posting. Read the employer’s full description below.
What they are looking for
- 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
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- 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
Employer 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
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