Human Subject Research Spec I

at  University of Rochester

QUALIFICATIONS:

• Bachelor’s Degree required
• No previous experience
• OR equivalent combination of education and experience (e.g. an Associate’s degree and completion of 6 months in the Human Subject Research Coordinator Trainee program) required.
• Word processing and data analysis software preferred.
• Professional Research Coordinator certification (SoCRA or ACRP) preferred.
  The University of Rochester is committed to fostering, cultivating, and preserving a culture of equity, diversity, and inclusion to advance the University’s mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, citizenship status, or any other status protected by law. This commitment extends to the administration of our policies, admissions, employment, access, and recruitment of candidates from underrepresented populations, veterans, and persons with disabilities consistent with these values and government contractor Affirmative Action obligations.

GENERAL PURPOSE:

Human Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated with human subject research. They will work under the supervision and guidance of the Principal Investigator (PI) for the particular study. This role will assume responsibility for less complex clinical research protocols, receiving guidance and instruction from senior level roles.