(Ol-664) - Cme-733 | Site Investigational Product Specialist

Johnson & Johnson is currently seeking a Site Investigational Product Specialist.
This position can be located remotely within the United States, preferably in the East Coast region.
At Johnson & Johnson, we believe health is everything.
Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal.
Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.
Position Overview: The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and procedure of the Investigational Product Preparation and Administration Instructions (IPPI), specific to drug administration in the area of clinical research.
Principal Responsibilities: Provide strategic input and recommendations at DPAT level as Subject Matter Experts (SME) on administration of IP, including ancillary supplies (AS) and different site practices for different routes of administration (Intravenous, Subcutaneous, Intramuscular, Oral, etc.)
Co-author of the IPPI with the Pharmacy Investigational Product Specialist (PIPS) and Drug Product Development Scientific Integrator/Technical Integrator (DPD SI/TI), coordinate review(s) and approval/sign-off of the IPPI document.
Review any modification of IPPI and other forms related to IP administration during the applicable phases of the trial.
Create and approve study list document for which the global IPPI is applicable.
Represent Global Development at DPAT meetings and closely collaborate with DPAT members on all IPPI-related topics.
Drive the gathering of collecting and maintaining global site intelligence on common materials for Ancillary Supplies (AS) as well as site practice via database inputs and oversight.
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