This is a fully remote position, open to applicants in Mexico.

📋 Description

• Responsible for overseeing the execution of studies at designated sites within the locality.

• Actively engages in Local Study Team (LST) meetings.

• Serves as the primary liaison with the study site.

• Monitors the conduct of the study to ensure its successful implementation.

• Accountable for the preparation, initiation, monitoring, and closure of assigned sites in clinical research.

⛳️ Requirements

• A minimum of 3 years of experience as an on-site Clinical Research Associate.

• Proficiency in both written and spoken English is essential.

• Fluency in the local language(s) is necessary.

• Strong understanding of international guidelines, specifically ICH-GCP.

• Familiarity with relevant local regulations is important.

• A Bachelor’s degree in a related field, preferably in life sciences.

🏝️ Benefits

• Health insurance coverage.

• Opportunities for professional development.

• Flexible work arrangements available.