Research Project Coordinator - Oncology

Overview

Experience the advantages of real career change

Join Piedmont to move your career in the right direction. Stay for the diverse teams youll love, a shared purpose, and schedule flexibility that frees you to live for what matters both in and outside of work. Youll feel valued, motivated to be your best, and recognized for your contributions to exceptional patient outcomes. Piedmont leaders are in your corner, invested in your success.

Our wellness programs and comprehensive total benefits and rewards meet your needs today and help you plan for the 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

• Bachelors 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

Work Experience

• 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

Licenses and Certifications

• None Required

Business Unit : Company Name

Piedmont Healthcare Corporate