REGULATORY INSTL REV BOARD CONSULTANT
BRONX, NY, US
Oversee regulatory operations for all hematology and heme malignancy clinical studies that are conducted through the Department of Medical Oncology, including, internal (investigator-initiated studies), external (e.g. NCI) and industrial protocols (pharmaceutical and biotechnology company studies).The benign hematology (including Sickle Cell) and heme malignancy clinical research programs will require a full-time IRB/regulatory manager who will be responsible for coordinating and maintaining all the regulatory documents and approvals for this program. This will involve working with closely with the Disease site leadership teams and daily interaction with sponsors and BRANY (3rd party IRB/Contracting)
Education/Skills:
Bachelor's Degree. Master's Degree preferred. One year's experience.
Knowledge of IRB, regulatory and NCI reporting.
Knowledge of clinical research within Oncology
This position is 100% grant funded.
Department: Oncology Bargaining Unit: Non Union Campus: MOSES Employment Status: Regular Full-Time Address: 1521 Jarrett Place, Bronx
Shift: Day Scheduled Hours: 8:30 AM-5 PM Req ID: 182683
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 of disability, 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.
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