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As a Quality Assurance Auditor II, you will develop and implement quality assurance strategies, conduct audits for compliance, collaborate with teams to resolve quality issues, review clinical trial documentation, and improve quality assurance practices.

The Senior Clinical Research Associate will coordinate activities for clinical studies, ensuring adherence to regulations and overseeing study documentation. Responsibilities include monitoring investigational sites, preparing regulatory submissions, and mentoring less experienced CRAs as needed, while traveling at least 60% for monitoring. Qualifications include 2-3 years of CRA experience and fluency in English.

As a Senior Clinical Research Associate, you will coordinate activities for study setup and monitoring while ensuring adherence to regulations. Responsibilities include preparing regulatory submissions, maintaining study documentation, and mentoring less experienced CRAs. You will work independently, manage sponsor queries, and travel for monitoring tasks.