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Overview
When you join Piedmont, you’re not just changing your work environment. We open doors to real change in the lives we touch — especially yours. We’re committed to bringing award-winning care to communities across Georgia and celebrating the strength our diversity creates. Together, we’re doing big things. One employee, one team, and one community at a time. Piedmont is a place where your work truly matters—and where you’re supported to do your best every day. We offer a collaborative culture, innovative resources, and leadership that is genuinely invested in your growth. With competitive benefits, wellness programs, and opportunities for advancement, you’ll have what you need to thrive now and build a strong future.Responsibilities
Responsible and accountable for the start-up activities of clinical research protocols initiated at Piedmont. Projects will span service lines and operational, clinical and financial areas and will be determined based on researchers' interest and engagement.Qualifications
Education- Bachelor’s Degree from a recognized college or university in a healthcare discipline Required or
- In Lieu of degree six (6) years of clinical research, healthcare or related field Required
- 5 years experience in all aspects of clinical research including study budgeting, phase I-IV research studies, screening, implementation and execution of research studies, regulatory and contracting Required or
- In lieu of degree eleven (11) years of experience in all aspects of clinical research including study budgeting, phase I-IV research studies, screening, implementation and execution of research studies, regulatory and contracting Required
- Clinical trial (investigational drug and/or device) experience Required and
- Familiarity with FDA regulations and IRB processes Required
- Community and academic experience in research Preferred
- None Required
Business Unit : Company Name
Piedmont Healthcare CorporateLearn more about this Employer on their Career Site
