RESEARCH NURSE SPECIALIST

The word “first” is inextricably linked with The Children's Hospital of Philadelphia. Since opening its doors in 1855 as the nation's first hospital devoted exclusively to the care of children, Children's Hospital has been the setting for many dramatic firsts, medical discoveries and breakthroughs that have formed the very foundations of pediatric medicine and benefited children throughout the world.

Today, The Children’s Hospital of Philadelphia is a growing network of facilities and resources that provides exceptional healthcare to all children, for every possible need.

Find out why we were ranked the #1 pediatric hospital in the nation by both Child Magazine and U.S. News & World Report. If you're looking to join a pediatric institution as your employer of choice, you need to look at the best in the nation.Coordinates clinical research activites within CHOP healthcare network. Provides specialized education concerning research studies and facilitates the conduct of clinical research within the CHOP healthcare network. Within the scope of clinical research protocols, participates in direct patient care accountable for adherence to all policies and procedures surrounding this process and for maintaining up to date knowledge on these policies from IRB, FDA, ICH, GCP or other sources.If you are a results-oriented individual with a passion for excellence, we invite you to learn more about the many opportunities and benefits The Children's Hospital of Philadelphia offers. Our employees enjoy a competitive compensation package that includes major medical, vision and dental benefits; tuition assistance; employer contribution retirement plan; work/life benefits; extensive training and staff development. And, of course, the opportunity to challenge themselves at a world-class institution.
REQUIREMENTS
B.S.N., registered nurse in the state of PA. Three years of research/clinical experience preferred. Successful performance in a high-intensity work environment. Excellent problem identification and problem solving skills. Flexibility and the ability to handle multiple tasks. Excellent interpersonal communication, organization, and managerial skills. Current knowledge of GCP and ICH guidelines essential. Definitions and reporting requirements for adverse events, IRB issues and guidelines, Elements of Informed Consent, FDA codes, and Regulatory issues preferred. Computer akills and a working knowledge of data management/analysis are desirable.