DescriptionEssential Functions- Responsible for submission of related documents to the appropriate research review committees and maintenance ofregulatory documentation.- Performs day-to-day activities related to clinical research studies including: recruit and screens participants, obtaininformed consent, educate participants regarding study requirements, and complete source documents and case reportforms (CRFs).- Conducts nursing assessments of research participants including appropriate reporting.- Documents, records and assimilates accurate participant records and study records to ensure documentation compliancewith sponsor guidelines, standard operating procedures (SOP) and internal and external regulatory agencies.- Establish and maintain communications with Investigator, Sponsor and internal constituents.Required For All Jobs- Performs other duties as assigned.- Complies with all policies and standards.- For specific duties and responsibilities, refer to documentation provided by the department during orientation.- Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients.Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHIin the workplace.Equal Opportunity Employer -- minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity