Senior In-house CRA

Key Responsibilities:

• Assists with investigator recruitment activities and site feasibility.
• Prepares and maintains investigator site files and trial master file (TMF).
• Serves as site contact for study management issues and coordinates study supplies.

Qualifications:

• Bachelor's degree in business, scientific, or healthcare discipline.
• 4 years of clinical trial or related experience.
• High proficiency in Microsoft Office and CTMS, TMF, and EDC systems.

Additional Information:

• Fully remote position based in Mexico with coverage across LATAM.
• Opportunity to work in a dynamic clinical research environment.
• Equal opportunity employer with commitment to diversity.