Positions range from junior to senior levels with regional opportunities in addition to in house positions.

Responsibilities include conducting Phase I - IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior staff in planning study conduct, designing case report forms (CRF's), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRF's from study sites, processing CRF's including data cleanup and classification of data, and completion of study summary.

Bachelor's Degree preferred with previous pharmaceutical research experience. Bachelors of Science in Nursing recommended.

Click Here To Search Current Job Openings!