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Precision Medicine Group
Senior Regulatory And Start Up Specialist
Remote · Argentina · Full time · Senior level
About the role
Lead regulatory and site start-up activities for clinical trials in Argentina. Ensure compliance with local and international regulations and support site activation readiness.
What you’ll do
• Prepare clinical trial submissions to authorities and ethics committees. • Review and adapt informed consent forms. • Support site contract management in budget and contract negotiation. • Act as subject matter expert and trainer for site start-up activities. • Maintain communication with project teams and regulatory bodies.
What you’ll bring
• Bachelor's degree in life sciences or related field. • 3.5+ years regulatory or site start-up experience. • Proficient English communication skills. • Legal authorization to work in Argentina. • Knowledge of Good Clinical Practice and ICH guidelines.
Life at Precision Medicine Group
Equal Opportunity Employer with commitment to diversity and inclusion. Provides reasonable accommodations for disabilities.
About Precision Medicine Group
Precision Medicine Group specializes in clinical trial regulatory and site start-up services across Latin America.