Clinical Research Associate III

Job Description:

Provides oversight to research staff and projects in assigned division. Collaborate with members of the research team in the organization, implementation and completion of clinical research trials. Oversee, create and maintain regulatory documents; organize protocol implementation and site initiation visits and conduct routine monitoring of clinical studies. Ensure that research projects are conducted in compliance with federal regulations, institutional/departmental guidelines and standards of Good Clinical Practice.

Requirements:

Required Education/Experience: Required Credentials: - N/A Preferred: - Master's Degree in a scientific discipline or related field - CCRA certification - Database management skills - Supervisory experience/skills


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Shannon works with sites across the nation that conduct cystic fibrosis trials to ensure that they have everything they need to perform their life-saving clinical research successfully.

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