The Site Engagement Liaison plays a central role in aligning clinical trial operations by serving as the primary point of contact between research sites, sponsors, and external partners. This position ensures clear, consistent communication and supports the effective delivery of clinical studies through proactive engagement and collaboration.
Key Responsibilities
- Act as a trusted liaison, facilitating two-way communication between clinical sites, sponsors, and third-party vendors
- Develop and sustain relationships with principal investigators, site coordinators, and research teams to promote study adherence and responsiveness
- Track and report on site performance indicators, providing timely updates to internal study teams
- Work with cross-functional teams to design and implement customized engagement plans based on study and site requirements
- Identify and act on opportunities to enhance site participation and performance through feedback and ongoing support
- Guide site personnel on study protocols, regulatory standards, and operational procedures to maintain compliance and data integrity
Qualifications
Candidates must hold a bachelor’s degree or equivalent and demonstrate prior experience in clinical research with a solid understanding of Good Clinical Practice. Fluency in English and any additional language required for local operations is essential. The ideal candidate will have therapeutic area knowledge and the ability to adapt quickly to evolving study needs. Strong organizational and self-management skills are critical for balancing multiple priorities effectively.
Prior experience as a Clinical Research Associate is beneficial but not required.
Work Environment
This role supports remote work arrangements for candidates based in Romania, offering flexibility while contributing to a global clinical operations framework. The organization promotes an inclusive, respectful workplace committed to sustainability, equity, and professional growth.
