BS or RN and 3 years of clinical experience, some of which includes site monitoring experience or BS or RN and 3 – 4 years of site coordination experience on multiple clinical studies or protocols;
Demonstrated core understanding of medical terminology, medical records and clinical trial activities;
Must have working knowledge of ICH-GCP guidelines, and FDA regulation as a result of clinical research experience;
Must be able to travel throughout the US 80% of the time;
Ability to monitor and coordinate multi-site research trials;
Excellent communication, interpersonal, decision making/problem solving and organizational skills;
Ability to work remotely as part of a team to initiate and implement appropriate quality control procedures;
Proficiency with Microsoft Office Products and electronic data capture (EDC) systems;
SOCRA or ACRP certificate is helpful, but not required.
NERI is an Equal Opportunity Employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identify and expression, age, disability, Vietnam era or other eligible veteran status, or any other protected factor.
Posted On -
3/31/2015 7:50:57 AM