As a

Lead Clinical Research Associate

, you will provide leadership, oversight, and mentorship to clinical study teams at a country or regional level. This role focuses on high-quality execution, compliance, and consistency in monitoring practices with minimal direct site management.

Key Responsibilities

- Monitor project timelines, patient enrollment, and data integrity.

- Review monitoring visit reports and ensure regulatory compliance.

- Act as the primary communication bridge between monitors, site management, and project leads.

- Lead project team calls and provide status updates to stakeholders.

- Supervise source data verification and risk management at the site level.





- Coordinate clinical supply management and essential study document reconciliation.

- Oversee CAPA development and implementation.

- Mentor and train newly promoted Lead CRAs and clinical staff.

Requirements

- Educational background in Life Sciences (MD, MPharm, RN, or equivalent).

- Minimum 4 years of site monitoring experience in general clinical projects.

- Experience with Phase II/III monitoring and site management in the US.

- Strong proficiency in Oncology, Cell/Gene Therapy, or GI preferred.

- Full working proficiency in English and MS Office applications.

📌 Lead Clinical Research Associate (Santiago)
🏢 Hunt Remotely
📍 Santiago