Job Description
Previous experience with clinical trials preferred.
Candidate will be responsible for providing support to the regulatory group of the Clinical Trials Office; assisting in logging, processing and entering protocols into database designed for tracking and reporting; assisting the Administrative Director and Coordinator of Protocol Development with protocol enforcement and related correspondence to IRB; preparing minutes for weekly regulatory meetings and coordinating site initiation visits; plus all duties as assigned.
Job Requirements
•Excellent communication skills are essential. Bachelor degree preferred.
•High School diploma with three years office experience or an equivalent combination of education and experience plus computer proficiency Microsoft Office required.
Please send resume and cover letter to:
Christopher.mcbride@nyumc.org
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