Senior Clinical Research Associate (Mexico)

Responsibilities:

• Independently oversees all aspects of study site management to ensure patient safety is protected.
• Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.
• Manages site start up procedures including the feasibility and recruitment of potential investigators.

Minimum Education & Experience:

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

Preferred Education & Experience:

• Graduate, postgraduate degree.
• Experience monitoring in rare and complex therapeutic areas.
• Experience monitoring EDC trials and EHR records.