We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials.
General Responsibilities:
- Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
- Participate in the development of improvement strategies for the site identification process, implementation thereof, as well as related training activities
Project Responsibilities:
- Define the main study objectives and the optimal site profile
- Create initial list of potential sites
- Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use
- In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities
- 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
- In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites
- Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed
