Job Description
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.
- Participate in project team meetings during study startup, as needed;
- Support the project team throughout study startup and further on.






