Clinical Research Coordinator

Position Summary

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.

• Bachelor’s degree in related field or equivalent combination of education and experience. (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)
• Phlebotomy 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)