Preventive Care β’ Specialized Care β’ Children's Hospital β’ Comprehensive Cancer Center β’ Digestive Health Center
10,000+
Yesterday
Preventive Care β’ Specialized Care β’ Children's Hospital β’ Comprehensive Cancer Center β’ Digestive Health Center
10,000+
β’ Conducts and develops all aspects of clinical, regulatory, business, and other research- related activities and documentation for clinical trials on behalf of the Levine Cancer Institute. β’ Assists Principal Investigator and team in evaluating feasibility of research studies. β’ Develops study budget in collaboration with team. β’ Coordinates documentation for regulatory requirements. β’ Coordinates trial-related activity of patients on protocols. β’ Monitors and reports significant study events including adverse events and protocol amendments. β’ Assists in data analysis and drafting of clinical study reports. β’ Educates patients and families about research studies, treatments, side effects and follow-up, as appropriate.
β’ Must hold a valid North Carolina or South Carolina (as applicable) Board of Nursing license. β’ Bachelor's Degree and 3 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or Master's Degree and 2 years of clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required; or a minimum of 6 years clinical research experience with a pharmaceutical company or Contract Research Organization or equivalent experience required with no degree. β’ Bachelor's Degree in Nursing or Master's Degree in Nursing or other health/science degree concentration preferred. β’ CPR certification required. β’ Previous experience in a healthcare setting preferred, especially cancer care and/or clinical research. β’ Certification in clinical research (SoCRA, ACRP, RAPS, etc.) preferred. β’ Supervisory experience preferred.
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