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.
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