Program Manager Clinical Research
Montefiore Medical Center | |
United States, New York, Bronx | |
Nov 20, 2025 | |
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City/State: Bronx, New YorkGrant Funded: YesDepartment: Cancer Clinical Trials OfficeWork Shift: DayWork Days: MON-FRIScheduled Hours: 9 AM-5:30 PMScheduled Daily Hours: 7.5 HOURSPay Range: $80,000.00-$100,000.00The Clinical ResearchProgramManager- Monitor, under the supervision of the Director of Quality Assurance, will provide compliance and quality assurance reviews for the Montefiore Einstein Cancer Clinical Trials Office. The Clinical ResearchProgramManager- Monitor will be responsible for all ongoing monitoring activities -patient case reviews, pharmacy reviews, regulatory reviews for Montefiore Einstein Cancer Center Investigator Initiated Trials (trials where MECC clinicians are the Sponsor Investigators/IND Holder). The CRM will provide routine reviews and determine if there are compliance concerns that warrant a formal of the trials. The duties of this position must be executed in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), the Montefiore Einstein Cancer Center Data and Safety Monitoring Plan (DSMP), and any other applicable regulatory requirements. The Clinical ResearchProgramManager- Monitor will work under the direction of the Director, Quality Assurance and will provide constant feedback on findings and evaluation of instituted Corrective and Preventative Action Plans (CAPA). The Clinical ResearchProgramManager- Monitor will serve as the Administrator for the MECC Data and Safety Monitoring Committee. In addition, the Clinical ResearchProgramManager- Monitor will work with the Director, Quality Assurance to develop and support an eligibility review process for all patients enrolled on cancer clinical studies. Requirements Bachelor's degree requires, Master's degree preferred 5 years of work experience required Minimum of 3 years of experience in clinical research CCRP/CCRC Certification preferred Prior experience with internal audits and/or FDA inspection preparations. Demonstrated knowledge proficiency of and adherence to federal (FDA, OHRP, GCP, etc.), state, and other regulatory standards, requirements, and guidelines related to clinical research Strong working knowledge of ongoing monitoring techniques (including criteria development and trending) Analytical and critical thinking skills to recognize trends Demonstrated communication, leadership, and team building skills: evidence of this should include dealing well with people, effective problem solving, appropriately confronting issues, motivating others as individuals and as groups, planning, organizing and directing the activities of others Demonstrated skill in working with minimal supervision Effective written and verbal communication Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center 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. | |
Nov 20, 2025