Shanghai, Shanghai, China
2 days ago
Clinical Regional Project Lead

Company Description

PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you

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 stagesReport project status updates and progress for a designated region; participate in Projects Review MeetingsEnsures consistency of all study processes across regions and identify regional differencesCommunicate with Global Project Managers and clientsManage project teams in the region, including team building, quality compliance, training and and monitoring of daily activitiesBe a point of contact for contractors and third party vendorsContribute to the development and update of project planning documents, essential documents, and project instructionsOversee maintenance of study-specific and corporate tracking systemsMight be involved in regional project oversight for APAC

QualificationsMPharm, RN or university/college degree in Life Sciences or an equivalent combination of education, training and experienceMinimum 4 years’ site monitoring experience in ChinaAt least 2 years’ experience as Lead MonitorExperience supervising clinical project activities and leading clinical project teamsExperience in oncology, gastroenterology, infectious diseases, autoimmune diseases, or any rare disease indication is preferableCommunication, presentation, and customer-service skillsTeam building, leadership and organizational skillsFull working proficiency in English and ChinsesProficiency in MS Office applications, including MS Project
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