Seeking a clinical trials study coordinator to join a team dedicated to obtaining FDA clearance for the company's molecular diagnostic pathogen identification products. The study coordinators primary responsibilities is to work closely with the Director of Regulatory Affairs to coordinate and manage all aspects of the clinical trials, including writing study protocols, obtaining all required IRB approvals, providing training and logistical support, performing monitoring activities, performing data analysis of the study results and writing reports.

This position requires travel to domestic and international trial sites. Must have strong organization and communication (oral and written) skills and attention to detail are required. Experience with project management and/or with regulatory submissions to the FDA is highly desirable.

Education: BS in scientific field and a minimum of 3 years of experience with molecular biology techniques.

Salary: Based upon experience, negotiable.

Work Hours: Full-time, flexible hours