About the job
Join PSI CRO as a dedicated Site Identification Specialist, where your expertise in forging strategic partnerships with clinical research sites will be pivotal in optimizing and advancing clinical trials.
This is a hybrid position based in Bucharest, Romania.
Key Responsibilities:
- Establish and nurture relationships with clinical sites to identify potential centers for clinical trials.
- Collaborate with Study Startup, Clinical Operations, and Process Improvement teams to maintain and enhance internal site databases.
Project Responsibilities:
- Lead site identification efforts, engaging in discussions about clinical trial protocols and gathering site identification questionnaires during the startup phase.
- Define core study objectives and develop an ideal site profile.
- Create an initial list of prospective sites.
- Work closely with project teams to refine strategies and methodologies for initial and follow-up site contacts based on indication, regional specifics, and technologies in use.
- Maintain a study site identification tracker in collaboration with the project team for further evaluation and selection activities.
- Coordinate with project teams to assess site identification progress and identify potential risks or issues impacting timelines or objectives.
- Conduct due diligence checks with Legal to ensure compliance with regulatory and legal frameworks for recommended investigators or clinical sites.
- Support the project team throughout the study startup and subsequent site identification rounds, providing additional information on sites/investigators as necessary.