Responsibilities
- Communicate and build relationship with clinical sites to identify potential centres for clinical trials.
- Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials.
- 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
Work Arrangement
Hybrid
Additional Information
- Hybrid role in Vienna, Austria
- Advanced English skills required
