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• Oncology clinical research coordinator will function independently and interdependently in collaboration with the clinical research nurse and other health care providers to promote ethical clinical practices in the conduct of clinical investigations.
• The coordinator must demonstrate an in-depth knowledge of federal regulations and guidance documents for the conduct of clinical trials to ensure human subject protection, compliance with protocol and regulatory requirements and the thorough collection, recording and maintenance of data and source documentation.
• Completion of regulatory and compliance forms, tracking of research training for participating specialty clinics, and maintenance of other research projects within the system, EPIC research module, and tracking and shipment of all protocol related submissions.
• This role functions to assist the clinical research nurse with care coordination of research patients and the research team in coordinating and facilitating the activities of all participants.

• Minimum of 1-2 years of Hospital or Clinic experience required.
• Oncology experience
• Society of Clinical Research Associate Certification (SOCRA) or Certified Clinical Research Professional Certification (CCRP).
• Bachelors degree in health sciences preferred.
• Clinical research experience, familiarity with federal regulations, GCP, HIPAA and IRB regulations.

• Shifts: M-F / day time shift
• Length of Assignment: 13 weeks then Right to Hire
• Pay Rate: TBD