Job Description
Coordinate clinical research studies for the principal investigators and coordinate and promote the research program within St. Elizabeth and the community. Responsible for networking with physicians to open studies, educating staff about current studies, educating clients about studies and obtaining informed consents. Responsibilities include screening and enrolling subjects in studies and managing their participation according to ethical, regulatory, and protocol specific requirements. Responsibilities also include data collection and regulatory compliance.
Demonstrate respect, dignity, kindness and empathy in each encounter with all patients, families, visitors and other employees regardless of cultural background.
Qualifications
Education, Credentials, Licenses:
Bachelor’s Degree in Nursing.
Graduate from an Accredited School of Nursing.
Licensed to practice nursing in the state where work is being performed.
Meet contact hour requirements for licensure, including all state-required courses.
Specialized Knowledge:
Understanding the research process.
Ability to effectively manage and prioritize multiple tasks while meting tight deadlines. Proficiency with Excel, Word, Outlook and PowerPoint is imperative. Ability to work with physicians, leadership, SEH/SEP associates, patients, external business partners, representatives of regulatory agencies and the general public.
Kind and Length of Experience:
5 year’s related experience in specialty area