Lead Clinical Investigator - Flexible Schedule

L4

celerionLincoln, NEtoday
Celerion is seeking a qualified Principal Investigator to oversee safety and conduct of clinical trials in line with FDA, GCP, and IRB requirements. The PI ensures subject safety, protocol adherence, and accurate data collection during all study phases. Responsibilities include protocol review, subject screening, SAE assessment, case report forms, safety reporting, and collaboration with sponsors and IRB. Candidates should have MD/DO, active license, and relevant clinical research experience,
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Level

MidL4

Location

Lincoln, NE

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)

Posted

today

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