**Job Description**

The Senior Clinical Research Monitor is responsible for performing ongoing internal reviews of research projects where human subject research is involved to ensure Investigators are compliant with federal regulations and guidelines governing clinical research, good clinical practices and institutional policies and procedures. The Senior Clinical Research Monitor mentors and advises less senior staff.

**Qualifications**

+ Bachelor's Degree in a Science related field; Masters Degree preferred
+ 7+ years of experience as a clinical research coordinator is required to include at least 5 years of progressive auditing/monitoring experience
+ ACRP (Association of Clinical Research Professionals) Certification strongly preferred

**Responsibilities**

+ Performs ongoing internal reviews of regulatory and essential documents, standard operating procedures (SOP), subject case files, protocol compliance, data and safety monitori...