Senior CRA - LatAm Clinical Trials Lead

Precision For Medicine; Argentina; On-site; ARS 127,190,291 - 164,599,200; Full time

Benefits offered by this job

Travel opportunities

Job summary

Precision Medicine Group in Argentina is expanding its Latin America capabilities and is seeking a Senior Clinical Research Associate to support critical studies across Argentina.

The Senior CRA will bring broad experience in start-up, on-site monitoring, and ongoing site management, while mentoring junior staff and collaborating with Clinical Trial Managers. Occasional travel to sites may be required to ensure trial integrity and regulatory compliance.

Qualifications

• 4-year college degree or equivalent in a scientific or healthcare discipline.
• 5+ years as a CRA in CRO or pharmaceutical/ biotech industry or equivalent.
• Graduate, postgraduate degree.
• Ability to communicate both verbally and in writing at the English proficiently (Professional level).

Responsibilities

• Oversees all aspects of study site management to ensure patient safety and data quality.
• Guides audit readiness and supports preparation for audit and follow-up actions.
• Maintains trial management tools, status reports, and site start-up procedures.
• Conducts on-site/remote monitoring visits per protocol and regulatory standards.
• Mentors junior staff and supports site staff training.
• Coordinates with CI/PMs for budget discussions and investigator contracts as needed.

Education

4-year college degree or equivalent in a scientific or healthcare discipline

5 years or more as a CRA in CRO or pharmaceutical/ biotech industry or equivalent

Graduate, postgraduate degree

English proficiency (Professional level)

Job description

Precision Medicine Group in Argentina is expanding its Latin America capabilities and is seeking a Senior Clinical Research Associate to support critical studies across Argentina.

The Senior CRA will bring broad experience in start-up, on-site monitoring, and ongoing site management, while mentoring junior staff and collaborating with Clinical Trial Managers. Occasional travel to sites may be required to ensure trial integrity and regulatory compliance.