Job Description
Please provide your CV in English.
The scope of responsibilities will include:
Constantly maintain and generate relations with Investigative Sites;Maintain and refine the internal site database in cooperation with Study Startup, Clinical Operations and Process Improvement;Participate in development of improvement strategies for the site identification process;Create the initial list of potential sites;Communicates with project teams to define strategy and methodology of initial and follow-up site contacts;In cooperation with the project team maintain a study site identification tracker;Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives;Perform due diligence check of regulatory limitations applicable to the recommended investigators or clinical sites.