Memorial Sloan-Kettering Cancer Center Clinical Research Supervisor - Multiple Myeloma Service, Department of Medicine in New York, New York

Clinical Research Supervisor – Multiple Myeloma Service, Department of Medicine

Job Posting Number: 20763

Research – Clinical

New York,NY

April 3, 2018

Company Overview:

At Memorial Sloan Kettering (MSK), we’re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we’re driving excellence and improving outcomes.

For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker’s Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor’s Employees’ Choice Best Place to Work for 2018. We’re treating cancer, one patient at a time. Join us and make a difference every day.

Job Details:

As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Supervisor manages the day-to-day activities of 6-10 Research Study Assistants in the Multiple Myeloma Service, Department of Medicine , ensuring efficient and effective operations. Responsible for direct supervision of protocol management activities including regulatory and data management of clinical research studies in Myeloma. Participates in special projects and task forces as determined by management. The Clinical Research Supervisor will supervise several research protocols, including investigator initiated trials, industry sponsored studies, as well as biospecimen protocols.

Responsibilities include:

  • Staff Management and Development – Participates in the orientation, training and supervision of Research Study Assistants. Participates in facilitating departmental trainings. Aligns staff and resources with appropriate protocols and research needs. Maintains workflow consistency amongst staff with standardized processes.

  • Operation Management – Ensures that workflow is managed and monitored to meet departmental and service needs. Assists Clinical Research Manager with protocol activation, especially with start-up activities. Monitors research portfolio for workload by appropriately managing and identifying service needs.

  • Quality Assurance – Performs regular audits to ensure that the data collected is complete and accurate and to ensure that the research project was carried out as outlined. Participates in the Institutional quality assurance audits.

  • Regulatory Compliance – Ensures that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written.

  • Data collection – Utilizes appropriate methodologies to oversee and collect patient/human subject information for research projects, databases, and/or protocols.

  • Data reporting – Generates reports to all necessary parties (institutional and federal) on the progress of the research project, database, or protocol. Prepares data for analysis, monitoring visits and audits.

  • Clinical Research Billing Management – Implements Principal Investigator’s decisions regarding Patient-Care Costs (both billable and non-billable), and ensures that research non-billable services are not billed to patients/human subjects or insurers. Assist manager with billing reconciliation.

  • Special Projects – Participates or coordinates on both interdepartmental and intradepartmental organization-wide research projects as requested. Provides leadership, organizational, creative, or clerical support to established and new research initiatives.

You need:

  • At least 2 years of relevant (clinical research) experience, or as determined by hiring manager.

  • At least one year’s supervisory experience strongly preferred.

  • Experience with Industrial, Investigator initiated and biospecimen protocols strongly preferred.

  • Must have a comprehensive 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).

  • Strong interpersonal, verbal and written communication skills. Ability to form strong and constructive internal as well as external professional relationships.

  • Effectively interacts with and collaborates at all levels in the organization.

  • Experience in collaboration with Investigators, relevant vendors, CROs and sponsors.

  • Detail oriented, excellent organizational skills.

  • Strong time management/project management skills.

  • Strong presentation skills.

  • Knowledge of oncology specific terminology is preferred.

  • Experience in the use of various electronic data management systems. Strong Data management skills, including database design preferred.

  • Basic knowledge of Microsoft suite (Power Point, Word, Access, Excel) and Teamshare.

MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision.

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.