Clinical Trial Manager - FSP
About This Gig
When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities : Manage external vendors and contract research organizations Prepare study documents such as the Monitoring Manual, Study Operations Manual, Source Data Verification Plan and Laboratory Manual Coordinate and be responsible for the design of study materials such as CRFs, patient diaries, study participation cards and source documents Assist with protocol development and study report completion Manage monitoring activities (may
About the Seller
Parexel
on Himalayas