Research Project Coordinator - Oncology

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)
• 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)
• Clinical trial (investigational drug and/or device) experience (Required and Familiarity with FDA regulations and IRB processes)
• Community and academic experience in research (Preferred)

Requirements

• Licenses and Certifications: None Required

Benefits

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.

Pay

N/A

Schedule

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Skills

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Company

Piedmont Healthcare