**Job Description**

Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and procedures. Mentors, trains and reviews the work of less experienced clinical research staff. Oversees the clinical assessments of the study subjects. Assists with protocol submissions, database enhancements, and budget preparation.

**Qualifications**

+ Bachelors degree in sciences or related field. Masters degree preferred
+ 5 years of clinical research

**Responsibilities**

+ Analyzes highly complex data gathered on clinical research studies.
+ Interprets complex clinical research data.
+ Conducts clinical testing, develops protocols and assures all protocol procedures are approved.
+ Prepares reports for presentation in conferences and seminars.
+ Mentors, trains and reviews the work of less experienced clinical research staff.
+ Dev...