IRB REGULATORY CONSULTANT
 Montefiore Medical Center | |
 United States, New York, Bronx | |
 Sep 24, 2024 | |
|
Oversee regulatory operations of clinical studies for one or more disease and modality teams. This includes internal (investigator-initiated studies), external (e.g. NCI) and industrial protocols (pharmaceutical and biotechnology company studies). Requirements Bachelor's degree required; Master's Degree preferred 1 year of related work experience Experience in working with FDA regulations and guidelines, 21 CFR, ICH guideline and initiatives governing regulatory operations and submissions (Pharma, Biotech, Medical Devices). Previous working or educational experience in the field regulatory reporting and compliance Department: Oncology Bargaining Unit:Non UnionCampus:MOSES Employment Status:Regular Full-TimeAddress:1525 Blondell Avenue, Bronx For positions that have only a rate listed, the displayedrate is the hiringrate but could be subject to change based on shift differential, experience, education or other relevant factors. To learn more about the "Montefiore Difference" - who we are at Montefiore and all that we have to offer our associates, please clickhere. Diversity, equity and inclusion are core values of Montefiore. We are committed to recruiting and creating an environment in which associates feel empowered to thrive and be their authentic selves through our inclusive culture. We welcome your interest and invite you to join us. Montefiore is an equal employment opportunity employer. Montefiore will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history ofdisability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status,or partnership status, or any other characteristic protected by law. #LI-VK1 | |