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See the original post from: Novo Nordisk
Summary:
Purpose Responsible for the support of assigned sites in accordance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, federal regulations and Standard Operating Procedures (SOPs). Collaboration with members within North America Clinical Trials (NACO) and various representatives in Clinical Medical Regulatory. May be responsible for monitoring assigned sites in accordance with GCP/ICH and Novo Nordisk Inc. (NNI) SOPs. Relationships Reports to a Manager/Sr. Manager/Associate Director of Site Management within NACO. Participate in multiple internal ...
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