Program Delivery Management - Nursing

The role will serve as a subject matter expert for nursing administration as it relates to the process and procedure of the IPPI (Investigational Product Preparation and Administration Instructions), specific to drug administration in the area of clinical research. The SIPS will play a lead role in the development of safe, efficient, and effective IP administration in clinical trials. The SIPS will be the key internal and external interface to ensure overall IPPI administration adherence. The SIPS will be co-author of the IPPI, and will be responsible for training slide development, training level assessment evaluation, and internal staff training. The SIPS will give input in ancillary supply selection and ancillary supply related questions, study feasibility, site assessment and mentoring for IPPI. He/she will contribute to continuous IPPI process improvement.



The SIPS will mainly focus on SIPS tasks for trials with an IPPI.



Deliverables:

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