Pay Range

Company Overview

The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe.

Please review important announcements about vaccination requirements and our upcoming EHR implementation by clicking here.

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Job Description

We are seeking Clinical Research Coordinators and Clinical Research Specialists to join us in the fight against cancer. Join us for the virtual interview day on April 9, and you will have the opportunity to meet with Supervisors, Managers and Principal Investigators who are actively working on research projects, studies and clinical trials!

We have exciting opportunities for remote, hybrid and onsite work!

You Are:

• A good decision-maker, with shown success at making timely decisions that keep the organization moving forward.
• Able to hold yourself and others accountable to achieve goals and live up to commitments.
• An effective communicator, capable of determining how best to reach different audiences and communicating based on that understanding.
• Willing to take action and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
• Resilient in recovering from setbacks and skilled at finding detours around obstacles..

As a Clinical Research Coordinator (Hybrid or Remote) You Will:

• Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials). This includes reviewing patient charts, existing databases, and other sources within a specified timeframe.
• Ensure data quality and integrity throughout the life of the study.
• Generate data reports and deliver to all vital parties on the progress of the research project, database, or protocol.
• Design and/or enhance databases, data forms and tools (e.g. patient/human subject calendars, schedules, tracking logs) to facilitate patient consent and specimen collection as needed for assigned research projects.
• Coordinate clinical research protocols and serve as the main point of contact, if applicable

As a Clinical Research Specialist (Onsite or Hybrid) You Will:

• Coordinate and perform tasks related to clinic
• Provide clinic support by assisting with patient management on study
• Support and help ensure complete regulatory compliance and data collection in clinic
• Coordinate meetings with the PIs and provide assistance to other CRCs as needed
• Assist with training new staff members and provide cross-coverage to various research teams

You Have:

• A minimum of a High School Diploma
• Commitment for at least 2 years

Are you ready to learn more about our Benefits?

Pay Ranges:

Clinical Research Coordinator $25.18-$37.75

Clinical Research Specialist $27.34-$42.36

Please click to find out more about MSK’s compensation philosophy!

Closing

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.