This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol. This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements.
Bachelors degree in related field (Required)
One year of clinical research experience or equivalent clinical research training program approved by Director, Clinical Research Operations (Required)
ACRP or SOCRA Clinical Research Certification (Preferred)
Clinical Research Training Certification (Preferred)
Proven ability to successfully coordinate multiple studies adhering to regulatory and institutional guidelines (Required)
Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care (Required)