Identify, select, initiate, & close-out appropriate investigational sites for clinical studies.
Monitor sites to ensure studies are carried out according to regulations.
Recruit investigators; independent & proactive coordination of all the necessary activities reqd to set up & monitor a study; deal with sponsor generated queries; act in a Lead role on a study & assume additional responsibilities as reqd by the Project Mgr.
Participate in training & mentoring new staff up to CRA level as appropriate.
Mentor & train other clinical staff as appropriate.
Req'd: BS or equiv. in medicine, science, or rltd & 3 yrs exp. w/active independent field monitoring & site mgmt, clinical research, & evaluating clinical data.
National & intl travel up to 70-80% for site visits.
Location/Region: San Diego, CA (US - 92122)