Small clinical trials department of busy dermatology practice in Troy, MI. Looking for individual who is experienced with all aspects of clinical trials: informed consent, performing study visits and procedures, EDC entry, IP accountability and contacting and scheduling potential subjects. Goal is to re-build and increase number of trials which will enable adding additional personnel. Self starter with minimal supervision needed.

Medical insurance, investment plan, vacation and holiday pay is available.

Experience as a clinical trials coordinator is mandatory, ideally more than 2 years.Highly motivated and willing to serve in all roles of running a trial. Able to conduct study visits, ship specimens, maintain logs. Detail oriented and accurate documentation required. Regulatory knowledge helpful but training available.

Able to work full time hours and flexible with possible early morning or early evening hours if needed.