At Memorial Sloan Kettering (MSK), were 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, were driving excellence and improving outcomes.Were treating cancer, one patient at a time.Join us and make a difference every day.

You will:

We have an exciting opportunity to join our dynamic team in theDepartment ofMedicineasClinical Research Supervisor (CRS) Thoracic Oncology Service.

As a CRS, you will supervise the day-to-day activities of the Clinical Research Associates (CRAs-protocol management) and the Clinical Research Coordinators (CRCs-data management) to ensure efficient and effective operations. You will be responsible for data management activities, data integrity, protocol and patient management associated with clinical research. You will manage several research protocols, including investigator-initiated trials, industry-sponsored studies, as well as bio-specimen protocols and work closely with service leadership and Principal Investigators.

You have:

• Staff Management and Development - Participate in the interviewing, hiring, orientating, training and supervision of CRAs & CRCs; participate in facilitating departmental trainings; align staff resources with appropriate protocols and research needs; andmaintain workflow consistency among staff with standardized processes.
• Operation Management - Ensure that workflow is managed and monitored to meet departmental and service needs; monitorresearch portfolio for workload by appropriately managing and identifying service needs.
• Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that theresearch project is carried out as planned.
• Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followedthroughout the course of a research project, database, or protocol. Ensure that research protocols are approved bythe Institutional Review Board/Privacy Board (IRB/PB) and followed as written.
• Data reporting - Generate reports to all necessary parties. Prepare data for analysis, monitoring visits and audits.
• Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wideresearch projects as requested. You will provide leadership, organizational, creative, or clerical support to establishedand new research initiatives.

You need:

• Bachelor's degree with at least 3 years of clinical research experience OR a high school diploma with 6 years of clinicalresearch experience.
• Supervisory experience and experience with high volume trials is strongly preferred. Knowledge of oncology-specific terminology is helpful.
• Strong time management/project management skills.
• Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.
• A good decision-maker, with shown success at making timely decisions that keep the organization moving forward.
• Eager to foster talent and support people in meeting their career goals and the organization's goals.

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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.

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