To apply medical knowledge and experience, under the direction of the onsite clinician to oversee and direct clinical course of research participants in clinical trials. Assess physical health and administer treatments throughout the study aligned with scope of practice delegated responsibilities. Oversee study conduct and assure study participant safety. Coordinate and manage care for participants enrolled in a clinical research trial. Will assist with management of patients within the Liver Institute.
Under the direction of the Principal Investigator, responsibilities will include, identify and recruitment of participants, obtaining informed consent, management of protocol related procedures, perform phlebotomies and insertion of IVs, prepare and maintain source documentation for phase 1-3 studies implemented at the Center. Participate in study visits, communicate with families, participants, referring physicians and other health care providers, Educating and guidance to participants and families to ensure compliance and retention of study participants, tracking and recording of adverse events, perform physical exams to ensure enrollment criteria and to track for any changes during study participation, diagnose and treat medical conditions such as allergic reactions and anaphylaxis during study drug administration, exacerbations of illness, formulate and evaluate treatment plans, manage common conditions such as allergic rhinitis, asthma and eczema, review home diaries and be available for on call advice and emergencies between clinic visits, administer rescue medications based on clinical judgment.
All duties are subject to change and/or be modified by Principal Investigator or Site Director.