About the job
The Regional Lead Site Coordinator plays a pivotal role in managing clinical trial activities across a designated group of medical institutions. This position involves collaborating closely with staff and Principal Investigators to ensure adherence to all applicable local and federal regulations, as well as overseeing protocol-specific tasks. Responsibilities include supervising site-level staff, assessing feasibility for potential clinical studies, facilitating research-related visits, coordinating logistics, and ensuring efficient patient flow during research activities.
Key responsibilities encompass:
- Maintaining clear communication between the Milestone One Manager, medical institution staff, and sponsors or CROs.
- Recruiting new site partners and identifying vendors for necessary services.
- Facilitating the evaluation process of proposed studies and ensuring timely responses to feasibility inquiries.
- Assisting in identifying new projects that align with the medical institution's interests and clinical needs.
- Actively participating in patient recruitment and eligibility confirmation according to study criteria.
- Conducting quality checks to ensure compliance with protocols and SOPs.
- Developing recruitment strategies and training programs to enhance site performance.
- Delivering training on clinical research best practices to staff.

