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.
Hybrid role in Vienna, Austria
This is the main responsibility of a site ID specialist
- Communicate and build relationship with clinical sites to identify potential centres for clinical trials.
- Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement
Project Responsibilities:
- 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