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FSP Site Intelligence Lead (Home-based)

Parexel International Corporation

Multiple Locations

•    Supports the build of the investigator database, collection of information supporting the definition of the ideal site for a study, identification of suitable sites for a study, and coordinates global efforts for site intelligence  

•    Acts as primary contact for the study team in the site intelligence process    

•    Participates in the site intelligence by leading the preparation of the country plan for the study (number of sites proposed, type of sites and key challenges) coordinating site intelligence resources to ensure timely completion of tasks and high quality  

•    Engages with therapeutic business units to support and deliver the implementation and delivery of specific site intelligence initiatives through good communication, clear implementation plans and explicit performance metrics to agreed timelines and quality 

•    Creates awareness by working as a cross functional team leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external. Initiatives will be diverse and may include technology and process improvement components   

•    Supports and maintains the development of relevant information libraries and communication materials to assist with site intelligence activities  

•    Additionally, runs operational and technical aspects of large global projects and assists with other Company systems activities related to the site intelligence  

•    Promotes a continuous improvement culture to streamline appropriate processes for maximum efficiency and productivity 

•    Maintains effective relationships with other platform lines, Business Units/Research Units, and enabling lines that facilitates effective portfolio delivery  

•    Support governance processes by providing site intelligence information leveraging existing data sources and organizational knowledge/expertise  

•    Partners with Study Teams, and Business Units/Research Units partners to improve overall study start up metrics and implement simple processes 

•    Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, system, and process related training 

•    Adheres to EP and Client SOPs and processes 

Job Requirements:

•    BS/Equivalent – 8 years’ experience in Clinical Research/Clinical Operations 

•    MS – 6 years’ experience in Clinical Research/Clinical Operations 

•    PhD/MD – 4 years’ experience in Clinical Research/Clinical Operations

Job posted: 2022-08-18

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