Career Center

We are:

The regional research program is responsible for research patient care for study participants enrolled in one or more of over 300+ protocols open in the regional outpatient MSK clinic locations. The long Island Clinical Research superviso r will supervise 16 Clinical Research Specialists at our Monmouth and Basking Ridge Regional Care Network and ensure research patient care is facilitated on study while ensuring compliance with all relevant regulatory guidelines from IRB, state and federal law, and Institutional SOPs. The Regional Research Program allows for expanded access to care in communities in the greater NYC area allowing MSK to remain a leader in providing top of the line research patient care.

We have an exciting opportunity to join our Regional Research Program for a Clinical Research Supervisor (CRS).

You will:

• Staff Management and Development - Participate in the orientation, training and supervision of CRSps; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes.
• Operation Management - Ensure that workflow is managed and supervised to meet departmental and service needs;
• Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research projects are carried out as planned.
• Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written.
• Data collection - Utilize appropriate methodologies to collect patient/human subject information for research projects, databases, and/or protocols.
• Data reporting - Generate reports to all vital parties. Prepare data for analysis, supervising visits and audits.
• Clinical Research Billing Management - Implement Principal Investigator's decisions regarding Patient-Care Costs.
• Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research initiatives.

You Are:

• Bachelor's degree with at least 3 years of clinical research experience OR a high school diploma with 6 years of clinical research experience
• Supervisory experience and experience with high volume trials is strongly preferred.
• Familiar and comfortable with human research protection protocols and guidelines
• Extensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA) is critical.
• Strong time management/project management skills.
• Knowledge of oncology-specific terminology is helpful.
• Experience in the use of various electronic data management systems. Strong Data management skills, including database design preferred.
• Basic knowledge of Microsoft suite (PowerPoint, Word, Access, Excel) and Teamshare

Hours:

• Monday - Friday, 9 AM - 5 PM. This role is onsite, which means that the individual will be required to come in to the office. Time to be split approximately between sites (Monmouth and Basking Ridge NJ)

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